Canonical Allele Identifier: CA367646110

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554266G>C (hg19) ; chr7:g.66089279G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089279G>C , CM000669.2:g.66089279G>C	GRCh38
NC_000007.13:g.65554266G>C , CM000669.1:g.65554266G>C	GRCh37
NC_000007.12:g.65191701G>C	NCBI36
NG_009288.1:g.18491G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.922G>C MANE Select	ENSP00000307188.9:p.Ala308Pro
ENST00000362000.10:c.727G>C	ENSP00000354710.6:p.Ala243Pro
ENST00000380839.9:c.844G>C	ENSP00000370219.4:p.Ala282Pro
ENST00000395331.4:c.918+104G>C	ENSP00000378740.3:n.918+104G>C
ENST00000395332.8:c.922G>C	ENSP00000378741.3:p.Ala308Pro
ENST00000488343.2:c.91G>C	ENSP00000500864.1:p.Ala31Pro
ENST00000671817.1:c.844G>C	ENSP00000500462.1:p.Ala282Pro
ENST00000672498.1:c.*221G>C	ENSP00000500227.1:n.*221G>C
ENST00000672586.1:n.1681G>C
ENST00000672676.1:n.1946G>C
ENST00000673149.1:n.734G>C
ENST00000673350.1:n.3039G>C
ENST00000673518.1:c.844G>C	ENSP00000499889.1:p.Ala282Pro
ENST00000304874.13:c.922G>C	ENSP00000307188.9:p.Ala308Pro
ENST00000380839.8:c.844G>C	ENSP00000370219.4:p.Ala282Pro
ENST00000395331.3:c.918+104G>C	ENSP00000378740.3:n.918+104G>C
ENST00000395332.7:c.922G>C	ENSP00000378741.3:p.Ala308Pro
ENST00000450043.2:c.235G>C	ENSP00000396527.2:p.Ala79Pro
ENST00000464970.1:n.41G>C
ENST00000488343.1:n.91G>C
ENST00000493708.5:n.403G>C
NM_000048.3:c.922G>C	NP_000039.2:p.Ala308Pro
NM_001024943.1:c.922G>C	NP_001020114.1:p.Ala308Pro
NM_001024944.1:c.918+104G>C	NP_001020115.1:n.918+104G>C
NM_001024946.1:c.844G>C	NP_001020117.1:p.Ala282Pro
NM_000048.4:c.922G>C MANE Select	NP_000039.2:p.Ala308Pro
NM_001024943.2:c.922G>C	NP_001020114.1:p.Ala308Pro
NM_001024944.2:c.918+104G>C	NP_001020115.1:n.918+104G>C
NM_001024946.2:c.844G>C	NP_001020117.1:p.Ala282Pro