Canonical Allele Identifier: CA367645691

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65554139A>C (hg19) ; chr7:g.66089152A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66089152A>C , CM000669.2:g.66089152A>C	GRCh38
NC_000007.13:g.65554139A>C , CM000669.1:g.65554139A>C	GRCh37
NC_000007.12:g.65191574A>C	NCBI36
NG_009288.1:g.18364A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.895A>C MANE Select	ENSP00000307188.9:p.Lys299Gln
ENST00000362000.10:c.700A>C	ENSP00000354710.6:p.Lys234Gln
ENST00000380839.9:c.817A>C	ENSP00000370219.4:p.Lys273Gln
ENST00000395331.4:c.895A>C	ENSP00000378740.3:p.Lys299Gln
ENST00000395332.8:c.895A>C	ENSP00000378741.3:p.Lys299Gln
ENST00000488343.2:c.64A>C	ENSP00000500864.1:p.Lys22Gln
ENST00000671817.1:c.817A>C	ENSP00000500462.1:p.Lys273Gln
ENST00000672498.1:c.*194A>C	ENSP00000500227.1:n.*194A>C
ENST00000672586.1:n.1654A>C
ENST00000672676.1:n.1919A>C
ENST00000673149.1:n.707A>C
ENST00000673350.1:n.3012A>C
ENST00000673518.1:c.817A>C	ENSP00000499889.1:p.Lys273Gln
ENST00000304874.13:c.895A>C	ENSP00000307188.9:p.Lys299Gln
ENST00000362000.9:c.700A>C	ENSP00000354710.5:p.Lys234Gln
ENST00000380839.8:c.817A>C	ENSP00000370219.4:p.Lys273Gln
ENST00000395331.3:c.895A>C	ENSP00000378740.3:p.Lys299Gln
ENST00000395332.7:c.895A>C	ENSP00000378741.3:p.Lys299Gln
ENST00000450043.2:c.208A>C	ENSP00000396527.2:p.Lys70Gln
ENST00000488343.1:n.64A>C
ENST00000493708.5:n.276A>C
NM_000048.3:c.895A>C	NP_000039.2:p.Lys299Gln
NM_001024943.1:c.895A>C	NP_001020114.1:p.Lys299Gln
NM_001024944.1:c.895A>C	NP_001020115.1:p.Lys299Gln
NM_001024946.1:c.817A>C	NP_001020117.1:p.Lys273Gln
NM_000048.4:c.895A>C MANE Select	NP_000039.2:p.Lys299Gln
NM_001024943.2:c.895A>C	NP_001020114.1:p.Lys299Gln
NM_001024944.2:c.895A>C	NP_001020115.1:p.Lys299Gln
NM_001024946.2:c.817A>C	NP_001020117.1:p.Lys273Gln