Canonical Allele Identifier: CA367645279

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65553880A>C (hg19) ; chr7:g.66088893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66088893A>C , CM000669.2:g.66088893A>C	GRCh38
NC_000007.13:g.65553880A>C , CM000669.1:g.65553880A>C	GRCh37
NC_000007.12:g.65191315A>C	NCBI36
NG_009288.1:g.18105A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.805A>C MANE Select	ENSP00000307188.9:p.Ser269Arg
ENST00000362000.10:c.610A>C	ENSP00000354710.6:p.Ser204Arg
ENST00000380839.9:c.727A>C	ENSP00000370219.4:p.Ser243Arg
ENST00000395331.4:c.805A>C	ENSP00000378740.3:p.Ser269Arg
ENST00000395332.8:c.805A>C	ENSP00000378741.3:p.Ser269Arg
ENST00000671817.1:c.727A>C	ENSP00000500462.1:p.Ser243Arg
ENST00000672498.1:c.*104A>C	ENSP00000500227.1:n.*104A>C
ENST00000672586.1:n.1564A>C
ENST00000672676.1:n.1829A>C
ENST00000673149.1:n.617A>C
ENST00000673350.1:n.2922A>C
ENST00000673518.1:c.727A>C	ENSP00000499889.1:p.Ser243Arg
ENST00000304874.13:c.805A>C	ENSP00000307188.9:p.Ser269Arg
ENST00000362000.9:c.610A>C	ENSP00000354710.5:p.Ser204Arg
ENST00000380839.8:c.727A>C	ENSP00000370219.4:p.Ser243Arg
ENST00000395331.3:c.805A>C	ENSP00000378740.3:p.Ser269Arg
ENST00000395332.7:c.805A>C	ENSP00000378741.3:p.Ser269Arg
ENST00000450043.2:c.118A>C	ENSP00000396527.2:p.Ser40Arg
ENST00000493708.5:n.186A>C
NM_000048.3:c.805A>C	NP_000039.2:p.Ser269Arg
NM_001024943.1:c.805A>C	NP_001020114.1:p.Ser269Arg
NM_001024944.1:c.805A>C	NP_001020115.1:p.Ser269Arg
NM_001024946.1:c.727A>C	NP_001020117.1:p.Ser243Arg
NM_000048.4:c.805A>C MANE Select	NP_000039.2:p.Ser269Arg
NM_001024943.2:c.805A>C	NP_001020114.1:p.Ser269Arg
NM_001024944.2:c.805A>C	NP_001020115.1:p.Ser269Arg
NM_001024946.2:c.727A>C	NP_001020117.1:p.Ser243Arg