Canonical Allele Identifier: CA455449943

Gene: ASL

Linked Data

• ClinVar Variation Id: 1923898
• ClinVar RCV Id: RCV002634679
• gnomAD v4: 7-66082385-C-A
• MyVariant Identifiers: chr7:g.65547372C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66082385C>A , CM000669.2:g.66082385C>A	GRCh38
NC_000007.13:g.65547372C>A , CM000669.1:g.65547372C>A	GRCh37
NC_000007.12:g.65184807C>A	NCBI36
NG_009288.1:g.11597C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.225C>A MANE Select	ENSP00000307188.9:p.Ala75=
ENST00000362000.10:c.30C>A	ENSP00000354710.6:p.Ala10=
ENST00000380839.9:c.225C>A	ENSP00000370219.4:p.Ala75=
ENST00000395331.4:c.225C>A	ENSP00000378740.3:p.Ala75=
ENST00000395332.8:c.225C>A	ENSP00000378741.3:p.Ala75=
ENST00000671817.1:c.225C>A	ENSP00000500462.1:p.Ala75=
ENST00000672498.1:c.225C>A	ENSP00000500227.1:p.Ala75=
ENST00000672586.1:n.130C>A
ENST00000672676.1:n.395C>A
ENST00000673350.1:n.473C>A
ENST00000673518.1:c.225C>A	ENSP00000499889.1:p.Ala75=
ENST00000673594.1:n.74C>A
ENST00000304874.13:c.225C>A	ENSP00000307188.9:p.Ala75=
ENST00000362000.9:c.30C>A	ENSP00000354710.5:p.Ala10=
ENST00000380839.8:c.225C>A	ENSP00000370219.4:p.Ala75=
ENST00000395331.3:c.225C>A	ENSP00000378740.3:p.Ala75=
ENST00000395332.7:c.225C>A	ENSP00000378741.3:p.Ala75=
ENST00000487982.5:n.291C>A
ENST00000496336.1:n.466C>A
NM_000048.3:c.225C>A	NP_000039.2:p.Ala75=
NM_001024943.1:c.225C>A	NP_001020114.1:p.Ala75=
NM_001024944.1:c.225C>A	NP_001020115.1:p.Ala75=
NM_001024946.1:c.225C>A	NP_001020117.1:p.Ala75=
NM_000048.4:c.225C>A MANE Select	NP_000039.2:p.Ala75=
NM_001024943.2:c.225C>A	NP_001020114.1:p.Ala75=
NM_001024944.2:c.225C>A	NP_001020115.1:p.Ala75=
NM_001024946.2:c.225C>A	NP_001020117.1:p.Ala75=