Canonical Allele Identifier: CA367645498

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554100C>T (hg19) ; chr7:g.66089113C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089113C>T , CM000669.2:g.66089113C>T	GRCh38
NC_000007.13:g.65554100C>T , CM000669.1:g.65554100C>T	GRCh37
NC_000007.12:g.65191535C>T	NCBI36
NG_009288.1:g.18325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.856C>T MANE Select	ENSP00000307188.9:p.Gln286Ter
ENST00000362000.10:c.661C>T	ENSP00000354710.6:p.Gln221Ter
ENST00000380839.9:c.778C>T	ENSP00000370219.4:p.Gln260Ter
ENST00000395331.4:c.856C>T	ENSP00000378740.3:p.Gln286Ter
ENST00000395332.8:c.856C>T	ENSP00000378741.3:p.Gln286Ter
ENST00000488343.2:c.25C>T	ENSP00000500864.1:p.Gln9Ter
ENST00000671817.1:c.778C>T	ENSP00000500462.1:p.Gln260Ter
ENST00000672498.1:c.*155C>T	ENSP00000500227.1:n.*155C>T
ENST00000672586.1:n.1615C>T
ENST00000672676.1:n.1880C>T
ENST00000673149.1:n.668C>T
ENST00000673350.1:n.2973C>T
ENST00000673518.1:c.778C>T	ENSP00000499889.1:p.Gln260Ter
ENST00000304874.13:c.856C>T	ENSP00000307188.9:p.Gln286Ter
ENST00000362000.9:c.661C>T	ENSP00000354710.5:p.Gln221Ter
ENST00000380839.8:c.778C>T	ENSP00000370219.4:p.Gln260Ter
ENST00000395331.3:c.856C>T	ENSP00000378740.3:p.Gln286Ter
ENST00000395332.7:c.856C>T	ENSP00000378741.3:p.Gln286Ter
ENST00000450043.2:c.169C>T	ENSP00000396527.2:p.Gln57Ter
ENST00000488343.1:n.25C>T
ENST00000493708.5:n.237C>T
NM_000048.3:c.856C>T	NP_000039.2:p.Gln286Ter
NM_001024943.1:c.856C>T	NP_001020114.1:p.Gln286Ter
NM_001024944.1:c.856C>T	NP_001020115.1:p.Gln286Ter
NM_001024946.1:c.778C>T	NP_001020117.1:p.Gln260Ter
NM_000048.4:c.856C>T MANE Select	NP_000039.2:p.Gln286Ter
NM_001024943.2:c.856C>T	NP_001020114.1:p.Gln286Ter
NM_001024944.2:c.856C>T	NP_001020115.1:p.Gln286Ter
NM_001024946.2:c.778C>T	NP_001020117.1:p.Gln260Ter