Canonical Allele Identifier: CA367639368

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65548112T>C (hg19) ; chr7:g.66083125T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66083125T>C , CM000669.2:g.66083125T>C	GRCh38
NC_000007.13:g.65548112T>C , CM000669.1:g.65548112T>C	GRCh37
NC_000007.12:g.65185547T>C	NCBI36
NG_009288.1:g.12337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.397T>C MANE Select	ENSP00000307188.9:p.Ser133Pro
ENST00000362000.10:c.202T>C	ENSP00000354710.6:p.Ser68Pro
ENST00000380839.9:c.397T>C	ENSP00000370219.4:p.Ser133Pro
ENST00000395331.4:c.397T>C	ENSP00000378740.3:p.Ser133Pro
ENST00000395332.8:c.397T>C	ENSP00000378741.3:p.Ser133Pro
ENST00000671817.1:c.397T>C	ENSP00000500462.1:p.Ser133Pro
ENST00000672498.1:c.397T>C	ENSP00000500227.1:p.Ser133Pro
ENST00000672586.1:n.302T>C
ENST00000672676.1:n.567T>C
ENST00000673149.1:n.209T>C
ENST00000673350.1:n.645T>C
ENST00000673518.1:c.397T>C	ENSP00000499889.1:p.Ser133Pro
ENST00000673594.1:n.246T>C
ENST00000304874.13:c.397T>C	ENSP00000307188.9:p.Ser133Pro
ENST00000362000.9:c.202T>C	ENSP00000354710.5:p.Ser68Pro
ENST00000380839.8:c.397T>C	ENSP00000370219.4:p.Ser133Pro
ENST00000395331.3:c.397T>C	ENSP00000378740.3:p.Ser133Pro
ENST00000395332.7:c.397T>C	ENSP00000378741.3:p.Ser133Pro
ENST00000487982.5:n.463T>C
ENST00000496336.1:n.778T>C
NM_000048.3:c.397T>C	NP_000039.2:p.Ser133Pro
NM_001024943.1:c.397T>C	NP_001020114.1:p.Ser133Pro
NM_001024944.1:c.397T>C	NP_001020115.1:p.Ser133Pro
NM_001024946.1:c.397T>C	NP_001020117.1:p.Ser133Pro
NM_000048.4:c.397T>C MANE Select	NP_000039.2:p.Ser133Pro
NM_001024943.2:c.397T>C	NP_001020114.1:p.Ser133Pro
NM_001024944.2:c.397T>C	NP_001020115.1:p.Ser133Pro
NM_001024946.2:c.397T>C	NP_001020117.1:p.Ser133Pro