Canonical Allele Identifier: CA455451065

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554268C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089281C>G , CM000669.2:g.66089281C>G	GRCh38
NC_000007.13:g.65554268C>G , CM000669.1:g.65554268C>G	GRCh37
NC_000007.12:g.65191703C>G	NCBI36
NG_009288.1:g.18493C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.924C>G MANE Select	ENSP00000307188.9:p.Ala308=
ENST00000362000.10:c.729C>G	ENSP00000354710.6:p.Ala243=
ENST00000380839.9:c.846C>G	ENSP00000370219.4:p.Ala282=
ENST00000395331.4:c.918+106C>G	ENSP00000378740.3:n.918+106C>G
ENST00000395332.8:c.924C>G	ENSP00000378741.3:p.Ala308=
ENST00000488343.2:c.93C>G	ENSP00000500864.1:p.Ala31=
ENST00000671817.1:c.846C>G	ENSP00000500462.1:p.Ala282=
ENST00000672498.1:c.*223C>G	ENSP00000500227.1:n.*223C>G
ENST00000672586.1:n.1683C>G
ENST00000672676.1:n.1948C>G
ENST00000673149.1:n.736C>G
ENST00000673350.1:n.3041C>G
ENST00000673518.1:c.846C>G	ENSP00000499889.1:p.Ala282=
ENST00000304874.13:c.924C>G	ENSP00000307188.9:p.Ala308=
ENST00000380839.8:c.846C>G	ENSP00000370219.4:p.Ala282=
ENST00000395331.3:c.918+106C>G	ENSP00000378740.3:n.918+106C>G
ENST00000395332.7:c.924C>G	ENSP00000378741.3:p.Ala308=
ENST00000450043.2:c.237C>G	ENSP00000396527.2:p.Ala79=
ENST00000464970.1:n.43C>G
ENST00000488343.1:n.93C>G
ENST00000493708.5:n.405C>G
NM_000048.3:c.924C>G	NP_000039.2:p.Ala308=
NM_001024943.1:c.924C>G	NP_001020114.1:p.Ala308=
NM_001024944.1:c.918+106C>G	NP_001020115.1:n.918+106C>G
NM_001024946.1:c.846C>G	NP_001020117.1:p.Ala282=
NM_000048.4:c.924C>G MANE Select	NP_000039.2:p.Ala308=
NM_001024943.2:c.924C>G	NP_001020114.1:p.Ala308=
NM_001024944.2:c.918+106C>G	NP_001020115.1:n.918+106C>G
NM_001024946.2:c.846C>G	NP_001020117.1:p.Ala282=