Canonical Allele Identifier: CA367638135

Gene: ASL

Linked Data

• dbSNP Id: rs1786514826
• MyVariant Identifiers: chr7:g.65546896A>C (hg19) ; chr7:g.66081909A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66081909A>C , CM000669.2:g.66081909A>C	GRCh38
NC_000007.13:g.65546896A>C , CM000669.1:g.65546896A>C	GRCh37
NC_000007.12:g.65184331A>C	NCBI36
NG_009288.1:g.11121A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.119A>C MANE Select	ENSP00000307188.9:p.Gln40Pro
ENST00000362000.10:c.13-459A>C	ENSP00000354710.6:n.13-459A>C
ENST00000380839.9:c.119A>C	ENSP00000370219.4:p.Gln40Pro
ENST00000395331.4:c.119A>C	ENSP00000378740.3:p.Gln40Pro
ENST00000395332.8:c.119A>C	ENSP00000378741.3:p.Gln40Pro
ENST00000671817.1:c.119A>C	ENSP00000500462.1:p.Gln40Pro
ENST00000672498.1:c.119A>C	ENSP00000500227.1:p.Gln40Pro
ENST00000672586.1:n.113-459A>C
ENST00000672676.1:n.289A>C
ENST00000673350.1:n.367A>C
ENST00000673518.1:c.119A>C	ENSP00000499889.1:p.Gln40Pro
ENST00000304874.13:c.119A>C	ENSP00000307188.9:p.Gln40Pro
ENST00000362000.9:c.13-459A>C	ENSP00000354710.5:n.13-459A>C
ENST00000380839.8:c.119A>C	ENSP00000370219.4:p.Gln40Pro
ENST00000395331.3:c.119A>C	ENSP00000378740.3:p.Gln40Pro
ENST00000395332.7:c.119A>C	ENSP00000378741.3:p.Gln40Pro
ENST00000487982.5:n.185A>C
ENST00000496336.1:n.360A>C
NM_000048.3:c.119A>C	NP_000039.2:p.Gln40Pro
NM_001024943.1:c.119A>C	NP_001020114.1:p.Gln40Pro
NM_001024944.1:c.119A>C	NP_001020115.1:p.Gln40Pro
NM_001024946.1:c.119A>C	NP_001020117.1:p.Gln40Pro
NM_000048.4:c.119A>C MANE Select	NP_000039.2:p.Gln40Pro
NM_001024943.2:c.119A>C	NP_001020114.1:p.Gln40Pro
NM_001024944.2:c.119A>C	NP_001020115.1:p.Gln40Pro
NM_001024946.2:c.119A>C	NP_001020117.1:p.Gln40Pro