Canonical Allele Identifier: CA455680059

Gene: ASL

Linked Data

• ClinVar Variation Id: 1085652
• ClinVar RCV Id: RCV001403113
• dbSNP Id: rs2115741935
• MyVariant Identifiers: chr7:g.65554147G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089160G>A , CM000669.2:g.66089160G>A	GRCh38
NC_000007.13:g.65554147G>A , CM000669.1:g.65554147G>A	GRCh37
NC_000007.12:g.65191582G>A	NCBI36
NG_009288.1:g.18372G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.903G>A MANE Select	ENSP00000307188.9:p.Gly301=
ENST00000362000.10:c.708G>A	ENSP00000354710.6:p.Gly236=
ENST00000380839.9:c.825G>A	ENSP00000370219.4:p.Gly275=
ENST00000395331.4:c.903G>A	ENSP00000378740.3:p.Gly301=
ENST00000395332.8:c.903G>A	ENSP00000378741.3:p.Gly301=
ENST00000488343.2:c.72G>A	ENSP00000500864.1:p.Gly24=
ENST00000671817.1:c.825G>A	ENSP00000500462.1:p.Gly275=
ENST00000672498.1:c.*202G>A	ENSP00000500227.1:n.*202G>A
ENST00000672586.1:n.1662G>A
ENST00000672676.1:n.1927G>A
ENST00000673149.1:n.715G>A
ENST00000673350.1:n.3020G>A
ENST00000673518.1:c.825G>A	ENSP00000499889.1:p.Gly275=
ENST00000304874.13:c.903G>A	ENSP00000307188.9:p.Gly301=
ENST00000362000.9:c.708G>A	ENSP00000354710.5:p.Gly236=
ENST00000380839.8:c.825G>A	ENSP00000370219.4:p.Gly275=
ENST00000395331.3:c.903G>A	ENSP00000378740.3:p.Gly301=
ENST00000395332.7:c.903G>A	ENSP00000378741.3:p.Gly301=
ENST00000450043.2:c.216G>A	ENSP00000396527.2:p.Gly72=
ENST00000488343.1:n.72G>A
ENST00000493708.5:n.284G>A
NM_000048.3:c.903G>A	NP_000039.2:p.Gly301=
NM_001024943.1:c.903G>A	NP_001020114.1:p.Gly301=
NM_001024944.1:c.903G>A	NP_001020115.1:p.Gly301=
NM_001024946.1:c.825G>A	NP_001020117.1:p.Gly275=
NM_000048.4:c.903G>A MANE Select	NP_000039.2:p.Gly301=
NM_001024943.2:c.903G>A	NP_001020114.1:p.Gly301=
NM_001024944.2:c.903G>A	NP_001020115.1:p.Gly301=
NM_001024946.2:c.825G>A	NP_001020117.1:p.Gly275=