Canonical Allele Identifier: CA367645406

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554082G>C (hg19) ; chr7:g.66089095G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089095G>C , CM000669.2:g.66089095G>C	GRCh38
NC_000007.13:g.65554082G>C , CM000669.1:g.65554082G>C	GRCh37
NC_000007.12:g.65191517G>C	NCBI36
NG_009288.1:g.18307G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.838G>C MANE Select	ENSP00000307188.9:p.Gly280Arg
ENST00000362000.10:c.643G>C	ENSP00000354710.6:p.Gly215Arg
ENST00000380839.9:c.760G>C	ENSP00000370219.4:p.Gly254Arg
ENST00000395331.4:c.838G>C	ENSP00000378740.3:p.Gly280Arg
ENST00000395332.8:c.838G>C	ENSP00000378741.3:p.Gly280Arg
ENST00000488343.2:c.7G>C	ENSP00000500864.1:p.Gly3Arg
ENST00000671817.1:c.760G>C	ENSP00000500462.1:p.Gly254Arg
ENST00000672498.1:c.*137G>C	ENSP00000500227.1:n.*137G>C
ENST00000672586.1:n.1597G>C
ENST00000672676.1:n.1862G>C
ENST00000673149.1:n.650G>C
ENST00000673350.1:n.2955G>C
ENST00000673518.1:c.760G>C	ENSP00000499889.1:p.Gly254Arg
ENST00000304874.13:c.838G>C	ENSP00000307188.9:p.Gly280Arg
ENST00000362000.9:c.643G>C	ENSP00000354710.5:p.Gly215Arg
ENST00000380839.8:c.760G>C	ENSP00000370219.4:p.Gly254Arg
ENST00000395331.3:c.838G>C	ENSP00000378740.3:p.Gly280Arg
ENST00000395332.7:c.838G>C	ENSP00000378741.3:p.Gly280Arg
ENST00000450043.2:c.151G>C	ENSP00000396527.2:p.Gly51Arg
ENST00000488343.1:n.7G>C
ENST00000493708.5:n.219G>C
NM_000048.3:c.838G>C	NP_000039.2:p.Gly280Arg
NM_001024943.1:c.838G>C	NP_001020114.1:p.Gly280Arg
NM_001024944.1:c.838G>C	NP_001020115.1:p.Gly280Arg
NM_001024946.1:c.760G>C	NP_001020117.1:p.Gly254Arg
NM_000048.4:c.838G>C MANE Select	NP_000039.2:p.Gly280Arg
NM_001024943.2:c.838G>C	NP_001020114.1:p.Gly280Arg
NM_001024944.2:c.838G>C	NP_001020115.1:p.Gly280Arg
NM_001024946.2:c.760G>C	NP_001020117.1:p.Gly254Arg