Canonical Allele Identifier: CA1025768771

Gene: ADSL

Linked Data

• gnomAD v3: 22-40350150-G-GTTTT
• gnomAD v4: 22-40350150-G-GTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40350150_40350151insTTTT , CM000684.2:g.40350150_40350151insTTTT	GRCh38
NC_000022.10:g.40746154_40746155insTTTT , CM000684.1:g.40746154_40746155insTTTT	GRCh37
NC_000022.9:g.39076100_39076101insTTTT	NCBI36
NG_007993.1:g.8651_8652insTTTT
NG_007993.2:g.8651_8652insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.357+115_357+116insTTTT	ENSP00000485462.2:n.357+115_357+116insTTTT
ENST00000623287.4:c.357+115_357+116insTTTT	ENSP00000485437.1:n.357+115_357+116insTTTT
ENST00000623632.4:c.357+115_357+116insTTTT	ENSP00000485288.2:n.357+115_357+116insTTTT
ENST00000625194.4:c.357+115_357+116insTTTT	ENSP00000485289.2:n.357+115_357+116insTTTT
ENST00000636124.1:n.49+2798_49+2799insTTTT
ENST00000636265.1:c.357+115_357+116insTTTT	ENSP00000490909.1:n.357+115_357+116insTTTT
ENST00000636714.1:c.357+115_357+116insTTTT	ENSP00000490946.1:n.357+115_357+116insTTTT
ENST00000637666.2:c.357+115_357+116insTTTT	ENSP00000489696.2:n.357+115_357+116insTTTT
ENST00000637669.1:c.357+115_357+116insTTTT	ENSP00000489728.1:n.357+115_357+116insTTTT
ENST00000638161.1:n.494+115_494+116insTTTT
ENST00000639722.1:c.*178+115_*178+116insTTTT	ENSP00000492828.1:n.*178+115_*178+116insTTTT
ENST00000675622.1:n.502_503insTTTT
ENST00000679609.1:c.357+115_357+116insTTTT	ENSP00000506592.1:n.357+115_357+116insTTTT
ENST00000679656.1:n.387+115_387+116insTTTT
ENST00000679723.1:c.357+115_357+116insTTTT	ENSP00000505155.1:n.357+115_357+116insTTTT
ENST00000680378.1:c.357+115_357+116insTTTT	ENSP00000505556.1:n.357+115_357+116insTTTT
ENST00000680444.1:c.357+115_357+116insTTTT	ENSP00000505298.1:n.357+115_357+116insTTTT
ENST00000680978.1:c.357+115_357+116insTTTT	ENSP00000505244.1:n.357+115_357+116insTTTT
ENST00000681159.1:n.416+115_416+116insTTTT
ENST00000216194.11:c.357+115_357+116insTTTT	ENSP00000216194.8:n.357+115_357+116insTTTT
ENST00000342312.9:c.357+115_357+116insTTTT	ENSP00000341429.6:n.357+115_357+116insTTTT
ENST00000466863.1:n.513_514insTTTT
ENST00000477111.2:n.387+115_387+116insTTTT
ENST00000623063.3:c.357+115_357+116insTTTT MANE Select	ENSP00000485525.1:n.357+115_357+116insTTTT
ENST00000623287.3:c.357+115_357+116insTTTT	ENSP00000485437.1:n.357+115_357+116insTTTT
ENST00000623632.3:c.357+115_357+116insTTTT	ENSP00000485288.1:n.357+115_357+116insTTTT
ENST00000623978.3:c.-183-2923_-183-2922insTTTT	ENSP00000485477.1:n.-183-2923_-183-2922insTTTT
ENST00000624474.1:c.357+115_357+116insTTTT	ENSP00000485286.1:n.357+115_357+116insTTTT
ENST00000624503.1:c.*88_*89insTTTT	ENSP00000485073.1:n.*88_*89insTTTT
NM_000026.2:c.357+115_357+116insTTTT	NP_000017.1:n.357+115_357+116insTTTT
NM_001123378.1:c.357+115_357+116insTTTT	NP_001116850.1:n.357+115_357+116insTTTT
XM_011529976.1:c.357+115_357+116insTTTT	XP_011528278.1:n.357+115_357+116insTTTT
XM_011529977.1:c.357+115_357+116insTTTT	XP_011528279.1:n.357+115_357+116insTTTT
XM_011529978.1:c.357+115_357+116insTTTT	XP_011528280.1:n.357+115_357+116insTTTT
XM_011529979.1:c.357+115_357+116insTTTT	XP_011528281.1:n.357+115_357+116insTTTT
XM_011529980.1:c.357+115_357+116insTTTT	XP_011528282.1:n.357+115_357+116insTTTT
XM_011529981.1:c.17+115_17+116insTTTT	XP_011528283.1:n.17+115_17+116insTTTT
XR_937824.1:n.416+115_416+116insTTTT
XR_937825.1:n.416+115_416+116insTTTT
XR_937826.1:n.416+115_416+116insTTTT
NM_000026.3:c.357+115_357+116insTTTT	NP_000017.1:n.357+115_357+116insTTTT
NM_001123378.2:c.357+115_357+116insTTTT	NP_001116850.1:n.357+115_357+116insTTTT
NM_001317923.1:c.165+115_165+116insTTTT	NP_001304852.1:n.165+115_165+116insTTTT
NM_001363840.1:c.357+115_357+116insTTTT	NP_001350769.1:n.357+115_357+116insTTTT
NR_134256.1:n.416+115_416+116insTTTT
XM_011529977.3:c.357+115_357+116insTTTT	XP_011528279.1:n.357+115_357+116insTTTT
XM_011529980.3:c.357+115_357+116insTTTT	XP_011528282.1:n.357+115_357+116insTTTT
XM_017028636.1:c.357+115_357+116insTTTT	XP_016884125.1:n.357+115_357+116insTTTT
XM_017028637.1:c.357+115_357+116insTTTT	XP_016884126.1:n.357+115_357+116insTTTT
XM_017028638.1:c.17+115_17+116insTTTT	XP_016884127.1:n.17+115_17+116insTTTT
XM_017028639.2:c.17+115_17+116insTTTT	XP_016884128.1:n.17+115_17+116insTTTT
XM_024452166.1:c.357+115_357+116insTTTT	XP_024307934.1:n.357+115_357+116insTTTT
XR_001755176.2:n.414+115_414+116insTTTT
XR_002958670.1:n.398+115_398+116insTTTT
XR_002958671.1:n.414+115_414+116insTTTT
XR_937825.3:n.414+115_414+116insTTTT
NM_000026.4:c.357+115_357+116insTTTT MANE Select	NP_000017.1:n.357+115_357+116insTTTT
NM_001363840.2:c.357+115_357+116insTTTT	NP_001350769.1:n.357+115_357+116insTTTT
NM_001123378.3:c.357+115_357+116insTTTT	NP_001116850.1:n.357+115_357+116insTTTT
NM_001317923.2:c.165+115_165+116insTTTT	NP_001304852.1:n.165+115_165+116insTTTT
NM_001363840.3:c.357+115_357+116insTTTT	NP_001350769.1:n.357+115_357+116insTTTT
NR_134256.2:n.416+115_416+116insTTTT