Canonical Allele Identifier: CA411646456

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40760306G>T (hg19) ; chr22:g.40364302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364302G>T , CM000684.2:g.40364302G>T	GRCh38
NC_000022.10:g.40760306G>T , CM000684.1:g.40760306G>T	GRCh37
NC_000022.9:g.39090252G>T	NCBI36
NG_007993.1:g.22803G>T
NG_007993.2:g.22803G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*522G>T	ENSP00000485462.2:n.*522G>T
ENST00000623287.4:c.*553G>T	ENSP00000485437.1:n.*553G>T
ENST00000623632.4:c.819G>T	ENSP00000485288.2:p.Glu273Asp
ENST00000625194.4:c.1170G>T	ENSP00000485289.2:p.Glu390Asp
ENST00000636265.1:c.1149G>T	ENSP00000490909.1:p.Glu383Asp
ENST00000636433.1:n.1150G>T
ENST00000636714.1:c.1128G>T	ENSP00000490946.1:p.Glu376Asp
ENST00000637666.2:c.1128G>T	ENSP00000489696.2:p.Glu376Asp
ENST00000637669.1:c.1128G>T	ENSP00000489728.1:p.Glu376Asp
ENST00000639722.1:c.*824G>T	ENSP00000492828.1:n.*824G>T
ENST00000674592.1:n.2642G>T
ENST00000675622.1:n.4195G>T
ENST00000679609.1:c.*738G>T	ENSP00000506592.1:n.*738G>T
ENST00000679656.1:n.1813G>T
ENST00000679723.1:c.1083G>T	ENSP00000505155.1:p.Glu361Asp
ENST00000679845.1:n.1436G>T
ENST00000679904.1:n.1524G>T
ENST00000680378.1:c.1215G>T	ENSP00000505556.1:p.Glu405Asp
ENST00000680444.1:c.*491G>T	ENSP00000505298.1:n.*491G>T
ENST00000680978.1:c.1128G>T	ENSP00000505244.1:p.Glu376Asp
ENST00000681003.1:n.591G>T
ENST00000681159.1:n.2532G>T
ENST00000216194.11:c.1170G>T	ENSP00000216194.8:p.Glu390Asp
ENST00000342312.9:c.1128G>T	ENSP00000341429.6:p.Glu376Asp
ENST00000623063.3:c.1128G>T MANE Select	ENSP00000485525.1:p.Glu376Asp
ENST00000625194.3:c.757G>T
NM_000026.2:c.1128G>T	NP_000017.1:p.Glu376Asp
NM_001123378.1:c.1128G>T	NP_001116850.1:p.Glu376Asp
XM_011529976.1:c.1128G>T	XP_011528278.1:p.Glu376Asp
XM_011529977.1:c.1128G>T	XP_011528279.1:p.Glu376Asp
XM_011529978.1:c.1128G>T	XP_011528280.1:p.Glu376Asp
XM_011529979.1:c.1128G>T	XP_011528281.1:p.Glu376Asp
XM_011529980.1:c.1128G>T	XP_011528282.1:p.Glu376Asp
XM_011529981.1:c.663G>T	XP_011528283.1:p.Glu221Asp
XM_011529982.1:c.297G>T	XP_011528284.1:p.Glu99Asp
XR_937824.1:n.1218G>T
XR_937825.1:n.1218G>T
NM_000026.3:c.1128G>T	NP_000017.1:p.Glu376Asp
NM_001123378.2:c.1128G>T	NP_001116850.1:p.Glu376Asp
NM_001317923.1:c.936G>T	NP_001304852.1:p.Glu312Asp
NM_001363840.1:c.1128G>T	NP_001350769.1:p.Glu376Asp
NR_134256.1:n.1218G>T
XM_011529977.3:c.1128G>T	XP_011528279.1:p.Glu376Asp
XM_011529980.3:c.1128G>T	XP_011528282.1:p.Glu376Asp
XM_017028636.1:c.1083G>T	XP_016884125.1:p.Glu361Asp
XM_017028637.1:c.1083G>T	XP_016884126.1:p.Glu361Asp
XM_017028638.1:c.663G>T	XP_016884127.1:p.Glu221Asp
XM_017028639.2:c.663G>T	XP_016884128.1:p.Glu221Asp
XM_017028640.1:c.297G>T	XP_016884129.1:p.Glu99Asp
XM_024452166.1:c.1083G>T	XP_024307934.1:p.Glu361Asp
XR_001755176.2:n.1370G>T
XR_002958670.1:n.1155G>T
XR_937825.3:n.1216G>T
NM_000026.4:c.1128G>T MANE Select	NP_000017.1:p.Glu376Asp
NM_001363840.2:c.1128G>T	NP_001350769.1:p.Glu376Asp
NM_001123378.3:c.1128G>T	NP_001116850.1:p.Glu376Asp
NM_001317923.2:c.936G>T	NP_001304852.1:p.Glu312Asp
NM_001363840.3:c.1128G>T	NP_001350769.1:p.Glu376Asp
NR_134256.2:n.1218G>T