Canonical Allele Identifier: CA841269797

Gene: ASL

Linked Data

• dbSNP Id: rs1279562234
• gnomAD v3: 7-66087595-G-A
• gnomAD v4: 7-66087595-G-A
• MyVariant Identifiers: chr7:g.65552582G>A (hg19) ; chr7:g.66087595G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66087595G>A , CM000669.2:g.66087595G>A	GRCh38
NC_000007.13:g.65552582G>A , CM000669.1:g.65552582G>A	GRCh37
NC_000007.12:g.65190017G>A	NCBI36
NG_009288.1:g.16807G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.656-134G>A MANE Select	ENSP00000307188.9:n.656-134G>A
ENST00000362000.10:c.461-134G>A	ENSP00000354710.6:n.461-134G>A
ENST00000380839.9:c.578-134G>A	ENSP00000370219.4:n.578-134G>A
ENST00000395331.4:c.656-134G>A	ENSP00000378740.3:n.656-134G>A
ENST00000395332.8:c.656-134G>A	ENSP00000378741.3:n.656-134G>A
ENST00000671817.1:c.578-134G>A	ENSP00000500462.1:n.578-134G>A
ENST00000672498.1:c.447-134G>A	ENSP00000500227.1:n.447-134G>A
ENST00000672586.1:n.1281G>A
ENST00000672676.1:n.1546G>A
ENST00000673149.1:n.468-134G>A
ENST00000673350.1:n.1624G>A
ENST00000673518.1:c.578-134G>A	ENSP00000499889.1:n.578-134G>A
ENST00000673594.1:n.713G>A
ENST00000304874.13:c.656-134G>A	ENSP00000307188.9:n.656-134G>A
ENST00000362000.9:c.461-134G>A	ENSP00000354710.5:n.461-134G>A
ENST00000380839.8:c.578-134G>A	ENSP00000370219.4:n.578-134G>A
ENST00000395331.3:c.656-134G>A	ENSP00000378740.3:n.656-134G>A
ENST00000395332.7:c.656-134G>A	ENSP00000378741.3:n.656-134G>A
NM_000048.3:c.656-134G>A	NP_000039.2:n.656-134G>A
NM_001024943.1:c.656-134G>A	NP_001020114.1:n.656-134G>A
NM_001024944.1:c.656-134G>A	NP_001020115.1:n.656-134G>A
NM_001024946.1:c.578-134G>A	NP_001020117.1:n.578-134G>A
NM_000048.4:c.656-134G>A MANE Select	NP_000039.2:n.656-134G>A
NM_001024943.2:c.656-134G>A	NP_001020114.1:n.656-134G>A
NM_001024944.2:c.656-134G>A	NP_001020115.1:n.656-134G>A
NM_001024946.2:c.578-134G>A	NP_001020117.1:n.578-134G>A