Canonical Allele Identifier: CA367638768

Gene: ASL

Linked Data

• dbSNP Id: rs1180118084
• gnomAD v2: 7-65547365-A-T
• gnomAD v4: 7-66082378-A-T
• MyVariant Identifiers: chr7:g.65547365A>T (hg19) ; chr7:g.66082378A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66082378A>T , CM000669.2:g.66082378A>T	GRCh38
NC_000007.13:g.65547365A>T , CM000669.1:g.65547365A>T	GRCh37
NC_000007.12:g.65184800A>T	NCBI36
NG_009288.1:g.11590A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.218A>T MANE Select	ENSP00000307188.9:p.Glu73Val
ENST00000362000.10:c.23A>T	ENSP00000354710.6:p.Glu8Val
ENST00000380839.9:c.218A>T	ENSP00000370219.4:p.Glu73Val
ENST00000395331.4:c.218A>T	ENSP00000378740.3:p.Glu73Val
ENST00000395332.8:c.218A>T	ENSP00000378741.3:p.Glu73Val
ENST00000671817.1:c.218A>T	ENSP00000500462.1:p.Glu73Val
ENST00000672498.1:c.218A>T	ENSP00000500227.1:p.Glu73Val
ENST00000672586.1:n.123A>T
ENST00000672676.1:n.388A>T
ENST00000673350.1:n.466A>T
ENST00000673518.1:c.218A>T	ENSP00000499889.1:p.Glu73Val
ENST00000673594.1:n.67A>T
ENST00000304874.13:c.218A>T	ENSP00000307188.9:p.Glu73Val
ENST00000362000.9:c.23A>T	ENSP00000354710.5:p.Glu8Val
ENST00000380839.8:c.218A>T	ENSP00000370219.4:p.Glu73Val
ENST00000395331.3:c.218A>T	ENSP00000378740.3:p.Glu73Val
ENST00000395332.7:c.218A>T	ENSP00000378741.3:p.Glu73Val
ENST00000487982.5:n.284A>T
ENST00000496336.1:n.459A>T
NM_000048.3:c.218A>T	NP_000039.2:p.Glu73Val
NM_001024943.1:c.218A>T	NP_001020114.1:p.Glu73Val
NM_001024944.1:c.218A>T	NP_001020115.1:p.Glu73Val
NM_001024946.1:c.218A>T	NP_001020117.1:p.Glu73Val
NM_000048.4:c.218A>T MANE Select	NP_000039.2:p.Glu73Val
NM_001024943.2:c.218A>T	NP_001020114.1:p.Glu73Val
NM_001024944.2:c.218A>T	NP_001020115.1:p.Glu73Val
NM_001024946.2:c.218A>T	NP_001020117.1:p.Glu73Val