Canonical Allele Identifier: CA1713929194

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66092861C= , CM000669.2:g.66092861C=	GRCh38
NC_000007.13:g.65557848C= , CM000669.1:g.65557848C=	GRCh37
NC_000007.12:g.65195283C=	NCBI36
NG_009288.1:g.22073C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.1344C= MANE Select	ENSP00000307188.9:p.Val448=
ENST00000362000.10:c.1149C=	ENSP00000354710.6:p.Val383=
ENST00000380839.9:c.1266C=	ENSP00000370219.4:p.Val422=
ENST00000395331.4:c.1284C=	ENSP00000378740.3:p.Val428=
ENST00000395332.8:c.1344C=	ENSP00000378741.3:p.Val448=
ENST00000488343.2:c.148-43C=	ENSP00000500864.1:n.148-43C=
ENST00000672498.1:c.*747C=	ENSP00000500227.1:n.*747C=
ENST00000672586.1:n.2103C=
ENST00000672676.1:n.2368C=
ENST00000673149.1:n.1156C=
ENST00000673350.1:n.3461C=
ENST00000673518.1:c.1266C=	ENSP00000499889.1:p.Val422=
ENST00000304874.13:c.1344C=	ENSP00000307188.9:p.Val448=
ENST00000380839.8:c.1266C=	ENSP00000370219.4:p.Val422=
ENST00000395331.3:c.1284C=	ENSP00000378740.3:p.Val428=
ENST00000395332.7:c.1344C=	ENSP00000378741.3:p.Val448=
ENST00000450043.2:c.563+198C=	ENSP00000396527.2:n.563+198C=
ENST00000464970.1:n.547C=
ENST00000488343.1:n.148-43C=
ENST00000493708.5:n.825C=
NM_000048.3:c.1344C=	NP_000039.2:p.Val448=
NM_001024943.1:c.1344C=	NP_001020114.1:p.Val448=
NM_001024944.1:c.1284C=	NP_001020115.1:p.Val428=
NM_001024946.1:c.1266C=	NP_001020117.1:p.Val422=
NM_000048.4:c.1344C= MANE Select	NP_000039.2:p.Val448=
NM_001024943.2:c.1344C=	NP_001020114.1:p.Val448=
NM_001024944.2:c.1284C=	NP_001020115.1:p.Val428=
NM_001024946.2:c.1266C=	NP_001020117.1:p.Val422=