Canonical Allele Identifier: CA367645532

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554112C>A (hg19) ; chr7:g.66089125C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089125C>A , CM000669.2:g.66089125C>A	GRCh38
NC_000007.13:g.65554112C>A , CM000669.1:g.65554112C>A	GRCh37
NC_000007.12:g.65191547C>A	NCBI36
NG_009288.1:g.18337C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.868C>A MANE Select	ENSP00000307188.9:p.Pro290Thr
ENST00000362000.10:c.673C>A	ENSP00000354710.6:p.Pro225Thr
ENST00000380839.9:c.790C>A	ENSP00000370219.4:p.Pro264Thr
ENST00000395331.4:c.868C>A	ENSP00000378740.3:p.Pro290Thr
ENST00000395332.8:c.868C>A	ENSP00000378741.3:p.Pro290Thr
ENST00000488343.2:c.37C>A	ENSP00000500864.1:p.Pro13Thr
ENST00000671817.1:c.790C>A	ENSP00000500462.1:p.Pro264Thr
ENST00000672498.1:c.*167C>A	ENSP00000500227.1:n.*167C>A
ENST00000672586.1:n.1627C>A
ENST00000672676.1:n.1892C>A
ENST00000673149.1:n.680C>A
ENST00000673350.1:n.2985C>A
ENST00000673518.1:c.790C>A	ENSP00000499889.1:p.Pro264Thr
ENST00000304874.13:c.868C>A	ENSP00000307188.9:p.Pro290Thr
ENST00000362000.9:c.673C>A	ENSP00000354710.5:p.Pro225Thr
ENST00000380839.8:c.790C>A	ENSP00000370219.4:p.Pro264Thr
ENST00000395331.3:c.868C>A	ENSP00000378740.3:p.Pro290Thr
ENST00000395332.7:c.868C>A	ENSP00000378741.3:p.Pro290Thr
ENST00000450043.2:c.181C>A	ENSP00000396527.2:p.Pro61Thr
ENST00000488343.1:n.37C>A
ENST00000493708.5:n.249C>A
NM_000048.3:c.868C>A	NP_000039.2:p.Pro290Thr
NM_001024943.1:c.868C>A	NP_001020114.1:p.Pro290Thr
NM_001024944.1:c.868C>A	NP_001020115.1:p.Pro290Thr
NM_001024946.1:c.790C>A	NP_001020117.1:p.Pro264Thr
NM_000048.4:c.868C>A MANE Select	NP_000039.2:p.Pro290Thr
NM_001024943.2:c.868C>A	NP_001020114.1:p.Pro290Thr
NM_001024944.2:c.868C>A	NP_001020115.1:p.Pro290Thr
NM_001024946.2:c.790C>A	NP_001020117.1:p.Pro264Thr