Canonical Allele Identifier: CA411648541

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40761025G>T (hg19) ; chr22:g.40365021G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365021G>T , CM000684.2:g.40365021G>T	GRCh38
NC_000022.10:g.40761025G>T , CM000684.1:g.40761025G>T	GRCh37
NC_000022.9:g.39090971G>T	NCBI36
NG_007993.1:g.23522G>T
NG_007993.2:g.23522G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*727G>T	ENSP00000485462.2:n.*727G>T
ENST00000623287.4:c.*758G>T	ENSP00000485437.1:n.*758G>T
ENST00000623632.4:c.1024G>T	ENSP00000485288.2:p.Asp342Tyr
ENST00000625194.4:c.1375G>T	ENSP00000485289.2:p.Asp459Tyr
ENST00000636433.1:n.1355G>T
ENST00000636714.1:c.1333G>T	ENSP00000490946.1:p.Asp445Tyr
ENST00000637666.2:c.1191+656G>T	ENSP00000489696.2:n.1191+656G>T
ENST00000637669.1:c.1333G>T	ENSP00000489728.1:p.Asp445Tyr
ENST00000639722.1:c.*1029G>T	ENSP00000492828.1:n.*1029G>T
ENST00000674592.1:n.2847G>T
ENST00000675622.1:n.4400G>T
ENST00000679609.1:c.*943G>T	ENSP00000506592.1:n.*943G>T
ENST00000679656.1:n.2018G>T
ENST00000679723.1:c.1288G>T	ENSP00000505155.1:p.Asp430Tyr
ENST00000679845.1:n.1641G>T
ENST00000679904.1:n.1729G>T
ENST00000680378.1:c.1420G>T	ENSP00000505556.1:p.Asp474Tyr
ENST00000680444.1:c.*696G>T	ENSP00000505298.1:n.*696G>T
ENST00000680978.1:c.1333G>T	ENSP00000505244.1:p.Asp445Tyr
ENST00000681003.1:n.796G>T
ENST00000681159.1:n.2737G>T
ENST00000216194.11:c.1375G>T	ENSP00000216194.8:p.Asp459Tyr
ENST00000342312.9:c.1191+656G>T	ENSP00000341429.6:n.1191+656G>T
ENST00000423176.6:c.60G>T
ENST00000623063.3:c.1333G>T MANE Select	ENSP00000485525.1:p.Asp445Tyr
ENST00000623387.1:n.464G>T
ENST00000623869.3:c.64G>T	ENSP00000485211.1:p.Asp22Tyr
ENST00000624027.1:c.60G>T
ENST00000625194.3:c.962G>T
NM_000026.2:c.1333G>T	NP_000017.1:p.Asp445Tyr
NM_001123378.1:c.1191+656G>T	NP_001116850.1:n.1191+656G>T
XM_011529976.1:c.1333G>T	XP_011528278.1:p.Asp445Tyr
XM_011529977.1:c.1333G>T	XP_011528279.1:p.Asp445Tyr
XM_011529978.1:c.1191+656G>T	XP_011528280.1:n.1191+656G>T
XM_011529979.1:c.1333G>T	XP_011528281.1:p.Asp445Tyr
XM_011529980.1:c.1191+656G>T	XP_011528282.1:n.1191+656G>T
XM_011529981.1:c.868G>T	XP_011528283.1:p.Asp290Tyr
XM_011529982.1:c.502G>T	XP_011528284.1:p.Asp168Tyr
XR_937824.1:n.1423G>T
XR_937825.1:n.1281+656G>T
NM_000026.3:c.1333G>T	NP_000017.1:p.Asp445Tyr
NM_001123378.2:c.1191+656G>T	NP_001116850.1:n.1191+656G>T
NM_001317923.1:c.1141G>T	NP_001304852.1:p.Asp381Tyr
NM_001363840.1:c.1333G>T	NP_001350769.1:p.Asp445Tyr
NR_134256.1:n.1423G>T
XM_011529977.3:c.1333G>T	XP_011528279.1:p.Asp445Tyr
XM_011529980.3:c.1191+656G>T	XP_011528282.1:n.1191+656G>T
XM_017028636.1:c.1288G>T	XP_016884125.1:p.Asp430Tyr
XM_017028637.1:c.1288G>T	XP_016884126.1:p.Asp430Tyr
XM_017028638.1:c.868G>T	XP_016884127.1:p.Asp290Tyr
XM_017028639.2:c.868G>T	XP_016884128.1:p.Asp290Tyr
XM_017028640.1:c.502G>T	XP_016884129.1:p.Asp168Tyr
XM_024452166.1:c.1146+656G>T	XP_024307934.1:n.1146+656G>T
XR_001755176.2:n.1575G>T
XR_002958670.1:n.1360G>T
XR_937825.3:n.1279+656G>T
NM_000026.4:c.1333G>T MANE Select	NP_000017.1:p.Asp445Tyr
NM_001363840.2:c.1333G>T	NP_001350769.1:p.Asp445Tyr
NM_001123378.3:c.1191+656G>T	NP_001116850.1:n.1191+656G>T
NM_001317923.2:c.1141G>T	NP_001304852.1:p.Asp381Tyr
NM_001363840.3:c.1333G>T	NP_001350769.1:p.Asp445Tyr
NR_134256.2:n.1423G>T