Canonical Allele Identifier: CA455450299

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65548156A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66083169A>T , CM000669.2:g.66083169A>T	GRCh38
NC_000007.13:g.65548156A>T , CM000669.1:g.65548156A>T	GRCh37
NC_000007.12:g.65185591A>T	NCBI36
NG_009288.1:g.12381A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.441A>T MANE Select	ENSP00000307188.9:p.Ala147=
ENST00000362000.10:c.246A>T	ENSP00000354710.6:p.Ala82=
ENST00000380839.9:c.441A>T	ENSP00000370219.4:p.Ala147=
ENST00000395331.4:c.441A>T	ENSP00000378740.3:p.Ala147=
ENST00000395332.8:c.441A>T	ENSP00000378741.3:p.Ala147=
ENST00000671817.1:c.441A>T	ENSP00000500462.1:p.Ala147=
ENST00000672498.1:c.441A>T	ENSP00000500227.1:p.Ala147=
ENST00000672586.1:n.346A>T
ENST00000672676.1:n.611A>T
ENST00000673149.1:n.253A>T
ENST00000673350.1:n.689A>T
ENST00000673518.1:c.441A>T	ENSP00000499889.1:p.Ala147=
ENST00000673594.1:n.290A>T
ENST00000304874.13:c.441A>T	ENSP00000307188.9:p.Ala147=
ENST00000362000.9:c.246A>T	ENSP00000354710.5:p.Ala82=
ENST00000380839.8:c.441A>T	ENSP00000370219.4:p.Ala147=
ENST00000395331.3:c.441A>T	ENSP00000378740.3:p.Ala147=
ENST00000395332.7:c.441A>T	ENSP00000378741.3:p.Ala147=
ENST00000487982.5:n.507A>T
ENST00000496336.1:n.822A>T
NM_000048.3:c.441A>T	NP_000039.2:p.Ala147=
NM_001024943.1:c.441A>T	NP_001020114.1:p.Ala147=
NM_001024944.1:c.441A>T	NP_001020115.1:p.Ala147=
NM_001024946.1:c.441A>T	NP_001020117.1:p.Ala147=
NM_000048.4:c.441A>T MANE Select	NP_000039.2:p.Ala147=
NM_001024943.2:c.441A>T	NP_001020114.1:p.Ala147=
NM_001024944.2:c.441A>T	NP_001020115.1:p.Ala147=
NM_001024946.2:c.441A>T	NP_001020117.1:p.Ala147=