Canonical Allele Identifier: CA4277144

Gene: ASL

Linked Data

• dbSNP Id: rs752388478
• ExAC: 7:65554037 C / A
• gnomAD v2: 7-65554037-C-A
• gnomAD v4: 7-66089050-C-A
• MyVariant Identifiers: chr7:g.65554037C>A (hg19) ; chr7:g.66089050C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089050C>A , CM000669.2:g.66089050C>A	GRCh38
NC_000007.13:g.65554037C>A , CM000669.1:g.65554037C>A	GRCh37
NC_000007.12:g.65191472C>A	NCBI36
NG_009288.1:g.18262C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.834-41C>A MANE Select	ENSP00000307188.9:n.834-41C>A
ENST00000362000.10:c.639-41C>A	ENSP00000354710.6:n.639-41C>A
ENST00000380839.9:c.756-41C>A	ENSP00000370219.4:n.756-41C>A
ENST00000395331.4:c.834-41C>A	ENSP00000378740.3:n.834-41C>A
ENST00000395332.8:c.834-41C>A	ENSP00000378741.3:n.834-41C>A
ENST00000488343.2:c.3-41C>A	ENSP00000500864.1:n.3-41C>A
ENST00000671817.1:c.756-41C>A	ENSP00000500462.1:n.756-41C>A
ENST00000672498.1:c.*133-41C>A	ENSP00000500227.1:n.*133-41C>A
ENST00000672586.1:n.1593-41C>A
ENST00000672676.1:n.1858-41C>A
ENST00000673149.1:n.646-41C>A
ENST00000673350.1:n.2951-41C>A
ENST00000673518.1:c.756-41C>A	ENSP00000499889.1:n.756-41C>A
ENST00000304874.13:c.834-41C>A	ENSP00000307188.9:n.834-41C>A
ENST00000362000.9:c.639-41C>A	ENSP00000354710.5:n.639-41C>A
ENST00000380839.8:c.756-41C>A	ENSP00000370219.4:n.756-41C>A
ENST00000395331.3:c.834-41C>A	ENSP00000378740.3:n.834-41C>A
ENST00000395332.7:c.834-41C>A	ENSP00000378741.3:n.834-41C>A
ENST00000450043.2:c.147-41C>A	ENSP00000396527.2:n.147-41C>A
ENST00000493708.5:n.215-41C>A
NM_000048.3:c.834-41C>A	NP_000039.2:n.834-41C>A
NM_001024943.1:c.834-41C>A	NP_001020114.1:n.834-41C>A
NM_001024944.1:c.834-41C>A	NP_001020115.1:n.834-41C>A
NM_001024946.1:c.756-41C>A	NP_001020117.1:n.756-41C>A
NM_000048.4:c.834-41C>A MANE Select	NP_000039.2:n.834-41C>A
NM_001024943.2:c.834-41C>A	NP_001020114.1:n.834-41C>A
NM_001024944.2:c.834-41C>A	NP_001020115.1:n.834-41C>A
NM_001024946.2:c.756-41C>A	NP_001020117.1:n.756-41C>A