Canonical Allele Identifier: CA367642137

Gene: ASL

Linked Data

• MyVariant Identifiers: chr7:g.65551636C>G (hg19) ; chr7:g.66086649C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66086649C>G , CM000669.2:g.66086649C>G	GRCh38
NC_000007.13:g.65551636C>G , CM000669.1:g.65551636C>G	GRCh37
NC_000007.12:g.65189071C>G	NCBI36
NG_009288.1:g.15861C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.511C>G MANE Select	ENSP00000307188.9:p.His171Asp
ENST00000362000.10:c.316C>G	ENSP00000354710.6:p.His106Asp
ENST00000380839.9:c.511C>G	ENSP00000370219.4:p.His171Asp
ENST00000395331.4:c.511C>G	ENSP00000378740.3:p.His171Asp
ENST00000395332.8:c.511C>G	ENSP00000378741.3:p.His171Asp
ENST00000671817.1:c.511C>G	ENSP00000500462.1:p.His171Asp
ENST00000672498.1:c.447-1080C>G	ENSP00000500227.1:n.447-1080C>G
ENST00000672586.1:n.416C>G
ENST00000672676.1:n.681C>G
ENST00000673149.1:n.323C>G
ENST00000673350.1:n.759C>G
ENST00000673518.1:c.511C>G	ENSP00000499889.1:p.His171Asp
ENST00000673594.1:n.360C>G
ENST00000304874.13:c.511C>G	ENSP00000307188.9:p.His171Asp
ENST00000362000.9:c.316C>G	ENSP00000354710.5:p.His106Asp
ENST00000380839.8:c.511C>G	ENSP00000370219.4:p.His171Asp
ENST00000395331.3:c.511C>G	ENSP00000378740.3:p.His171Asp
ENST00000395332.7:c.511C>G	ENSP00000378741.3:p.His171Asp
ENST00000487982.5:n.577C>G
NM_000048.3:c.511C>G	NP_000039.2:p.His171Asp
NM_001024943.1:c.511C>G	NP_001020114.1:p.His171Asp
NM_001024944.1:c.511C>G	NP_001020115.1:p.His171Asp
NM_001024946.1:c.511C>G	NP_001020117.1:p.His171Asp
NM_000048.4:c.511C>G MANE Select	NP_000039.2:p.His171Asp
NM_001024943.2:c.511C>G	NP_001020114.1:p.His171Asp
NM_001024944.2:c.511C>G	NP_001020115.1:p.His171Asp
NM_001024946.2:c.511C>G	NP_001020117.1:p.His171Asp