Canonical Allele Identifier: CA753184085

Gene: ADSL

Linked Data

• dbSNP Id: rs1327170607
• gnomAD v3: 22-40364817-CT-C
• gnomAD v4: 22-40364817-CT-C
• MyVariant Identifiers: chr22:g.40760822del (hg19) ; chr22:g.40364818del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364822del , CM000684.2:g.40364822del	GRCh38
NC_000022.10:g.40760826del , CM000684.1:g.40760826del	GRCh37
NC_000022.9:g.39090772del	NCBI36
NG_007993.1:g.23323del
NG_007993.2:g.23323del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*586-58del	ENSP00000485462.2:n.*586-58del
ENST00000623287.4:c.*617-58del	ENSP00000485437.1:n.*617-58del
ENST00000623632.4:c.883-58del	ENSP00000485288.2:n.883-58del
ENST00000625194.4:c.1234-58del	ENSP00000485289.2:n.1234-58del
ENST00000636433.1:n.1214-58del
ENST00000636714.1:c.1192-58del	ENSP00000490946.1:n.1192-58del
ENST00000637666.2:c.1191+457del	ENSP00000489696.2:n.1191+457del
ENST00000637669.1:c.1192-58del	ENSP00000489728.1:n.1192-58del
ENST00000639722.1:c.*888-58del	ENSP00000492828.1:n.*888-58del
ENST00000674592.1:n.2706-58del
ENST00000675622.1:n.4259-58del
ENST00000679609.1:c.*802-58del	ENSP00000506592.1:n.*802-58del
ENST00000679656.1:n.1877-58del
ENST00000679723.1:c.1147-58del	ENSP00000505155.1:n.1147-58del
ENST00000679845.1:n.1500-58del
ENST00000679904.1:n.1588-58del
ENST00000680378.1:c.1279-58del	ENSP00000505556.1:n.1279-58del
ENST00000680444.1:c.*555-58del	ENSP00000505298.1:n.*555-58del
ENST00000680978.1:c.1192-58del	ENSP00000505244.1:n.1192-58del
ENST00000681003.1:n.655-58del
ENST00000681159.1:n.2596-58del
ENST00000216194.11:c.1234-58del	ENSP00000216194.8:n.1234-58del
ENST00000342312.9:c.1191+457del	ENSP00000341429.6:n.1191+457del
ENST00000623063.3:c.1192-58del MANE Select	ENSP00000485525.1:n.1192-58del
ENST00000623387.1:n.265del
ENST00000625194.3:c.821-58del
NM_000026.2:c.1192-58del	NP_000017.1:n.1192-58del
NM_001123378.1:c.1191+457del	NP_001116850.1:n.1191+457del
XM_011529976.1:c.1192-58del	XP_011528278.1:n.1192-58del
XM_011529977.1:c.1192-58del	XP_011528279.1:n.1192-58del
XM_011529978.1:c.1191+457del	XP_011528280.1:n.1191+457del
XM_011529979.1:c.1192-58del	XP_011528281.1:n.1192-58del
XM_011529980.1:c.1191+457del	XP_011528282.1:n.1191+457del
XM_011529981.1:c.727-58del	XP_011528283.1:n.727-58del
XM_011529982.1:c.361-58del	XP_011528284.1:n.361-58del
XR_937824.1:n.1282-58del
XR_937825.1:n.1281+457del
NM_000026.3:c.1192-58del	NP_000017.1:n.1192-58del
NM_001123378.2:c.1191+457del	NP_001116850.1:n.1191+457del
NM_001317923.1:c.1000-58del	NP_001304852.1:n.1000-58del
NM_001363840.1:c.1192-58del	NP_001350769.1:n.1192-58del
NR_134256.1:n.1282-58del
XM_011529977.3:c.1192-58del	XP_011528279.1:n.1192-58del
XM_011529980.3:c.1191+457del	XP_011528282.1:n.1191+457del
XM_017028636.1:c.1147-58del	XP_016884125.1:n.1147-58del
XM_017028637.1:c.1147-58del	XP_016884126.1:n.1147-58del
XM_017028638.1:c.727-58del	XP_016884127.1:n.727-58del
XM_017028639.2:c.727-58del	XP_016884128.1:n.727-58del
XM_017028640.1:c.361-58del	XP_016884129.1:n.361-58del
XM_024452166.1:c.1146+457del	XP_024307934.1:n.1146+457del
XR_001755176.2:n.1434-58del
XR_002958670.1:n.1219-58del
XR_937825.3:n.1279+457del
NM_000026.4:c.1192-58del MANE Select	NP_000017.1:n.1192-58del
NM_001363840.2:c.1192-58del	NP_001350769.1:n.1192-58del
NM_001123378.3:c.1191+457del	NP_001116850.1:n.1191+457del
NM_001317923.2:c.1000-58del	NP_001304852.1:n.1000-58del
NM_001363840.3:c.1192-58del	NP_001350769.1:n.1192-58del
NR_134256.2:n.1282-58del