Canonical Allele Identifier: CA455452064

Gene: ASL

Linked Data

• dbSNP Id: rs1208547893
• gnomAD v2: 7-65557761-G-T
• gnomAD v4: 7-66092774-G-T
• MyVariant Identifiers: chr7:g.65557761G>T (hg19) ; chr7:g.66092774G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66092774G>T , CM000669.2:g.66092774G>T	GRCh38
NC_000007.13:g.65557761G>T , CM000669.1:g.65557761G>T	GRCh37
NC_000007.12:g.65195196G>T	NCBI36
NG_009288.1:g.21986G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.1257G>T MANE Select	ENSP00000307188.9:p.Leu419=
ENST00000362000.10:c.1062G>T	ENSP00000354710.6:p.Leu354=
ENST00000380839.9:c.1179G>T	ENSP00000370219.4:p.Leu393=
ENST00000395331.4:c.1197G>T	ENSP00000378740.3:p.Leu399=
ENST00000395332.8:c.1257G>T	ENSP00000378741.3:p.Leu419=
ENST00000488343.2:c.148-130G>T	ENSP00000500864.1:n.148-130G>T
ENST00000672498.1:c.*660G>T	ENSP00000500227.1:n.*660G>T
ENST00000672586.1:n.2016G>T
ENST00000672676.1:n.2281G>T
ENST00000673149.1:n.1069G>T
ENST00000673350.1:n.3374G>T
ENST00000673518.1:c.1179G>T	ENSP00000499889.1:p.Leu393=
ENST00000304874.13:c.1257G>T	ENSP00000307188.9:p.Leu419=
ENST00000380839.8:c.1179G>T	ENSP00000370219.4:p.Leu393=
ENST00000395331.3:c.1197G>T	ENSP00000378740.3:p.Leu399=
ENST00000395332.7:c.1257G>T	ENSP00000378741.3:p.Leu419=
ENST00000450043.2:c.563+111G>T	ENSP00000396527.2:n.563+111G>T
ENST00000464970.1:n.460G>T
ENST00000488343.1:n.148-130G>T
ENST00000493708.5:n.738G>T
NM_000048.3:c.1257G>T	NP_000039.2:p.Leu419=
NM_001024943.1:c.1257G>T	NP_001020114.1:p.Leu419=
NM_001024944.1:c.1197G>T	NP_001020115.1:p.Leu399=
NM_001024946.1:c.1179G>T	NP_001020117.1:p.Leu393=
NM_000048.4:c.1257G>T MANE Select	NP_000039.2:p.Leu419=
NM_001024943.2:c.1257G>T	NP_001020114.1:p.Leu419=
NM_001024944.2:c.1197G>T	NP_001020115.1:p.Leu399=
NM_001024946.2:c.1179G>T	NP_001020117.1:p.Leu393=