Canonical Allele Identifier: CA455680050

Gene: ASL

Linked Data

• gnomAD v4: 7-66089146-C-A
• MyVariant Identifiers: chr7:g.65554133C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089146C>A , CM000669.2:g.66089146C>A	GRCh38
NC_000007.13:g.65554133C>A , CM000669.1:g.65554133C>A	GRCh37
NC_000007.12:g.65191568C>A	NCBI36
NG_009288.1:g.18358C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.889C>A MANE Select	ENSP00000307188.9:p.Arg297=
ENST00000362000.10:c.694C>A	ENSP00000354710.6:p.Arg232=
ENST00000380839.9:c.811C>A	ENSP00000370219.4:p.Arg271=
ENST00000395331.4:c.889C>A	ENSP00000378740.3:p.Arg297=
ENST00000395332.8:c.889C>A	ENSP00000378741.3:p.Arg297=
ENST00000488343.2:c.58C>A	ENSP00000500864.1:p.Arg20=
ENST00000671817.1:c.811C>A	ENSP00000500462.1:p.Arg271=
ENST00000672498.1:c.*188C>A	ENSP00000500227.1:n.*188C>A
ENST00000672586.1:n.1648C>A
ENST00000672676.1:n.1913C>A
ENST00000673149.1:n.701C>A
ENST00000673350.1:n.3006C>A
ENST00000673518.1:c.811C>A	ENSP00000499889.1:p.Arg271=
ENST00000304874.13:c.889C>A	ENSP00000307188.9:p.Arg297=
ENST00000362000.9:c.694C>A	ENSP00000354710.5:p.Arg232=
ENST00000380839.8:c.811C>A	ENSP00000370219.4:p.Arg271=
ENST00000395331.3:c.889C>A	ENSP00000378740.3:p.Arg297=
ENST00000395332.7:c.889C>A	ENSP00000378741.3:p.Arg297=
ENST00000450043.2:c.202C>A	ENSP00000396527.2:p.Arg68=
ENST00000488343.1:n.58C>A
ENST00000493708.5:n.270C>A
NM_000048.3:c.889C>A	NP_000039.2:p.Arg297=
NM_001024943.1:c.889C>A	NP_001020114.1:p.Arg297=
NM_001024944.1:c.889C>A	NP_001020115.1:p.Arg297=
NM_001024946.1:c.811C>A	NP_001020117.1:p.Arg271=
NM_000048.4:c.889C>A MANE Select	NP_000039.2:p.Arg297=
NM_001024943.2:c.889C>A	NP_001020114.1:p.Arg297=
NM_001024944.2:c.889C>A	NP_001020115.1:p.Arg297=
NM_001024946.2:c.811C>A	NP_001020117.1:p.Arg271=