Canonical Allele Identifier: CA1713928483

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66092587G= , CM000669.2:g.66092587G=	GRCh38
NC_000007.13:g.65557574G= , CM000669.1:g.65557574G=	GRCh37
NC_000007.12:g.65195009G=	NCBI36
NG_009288.1:g.21799G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304874.14:c.1174G= MANE Select	ENSP00000307188.9:p.Gly392=
ENST00000362000.10:c.979G=	ENSP00000354710.6:p.Gly327=
ENST00000380839.9:c.1096G=	ENSP00000370219.4:p.Gly366=
ENST00000395331.4:c.1114G=	ENSP00000378740.3:p.Gly372=
ENST00000395332.8:c.1174G=	ENSP00000378741.3:p.Gly392=
ENST00000488343.2:c.148-317G=	ENSP00000500864.1:n.148-317G=
ENST00000672498.1:c.*473G=	ENSP00000500227.1:n.*473G=
ENST00000672586.1:n.1933G=
ENST00000672676.1:n.2198G=
ENST00000673149.1:n.986G=
ENST00000673350.1:n.3291G=
ENST00000673518.1:c.1096G=	ENSP00000499889.1:p.Gly366=
ENST00000304874.13:c.1174G=	ENSP00000307188.9:p.Gly392=
ENST00000380839.8:c.1096G=	ENSP00000370219.4:p.Gly366=
ENST00000395331.3:c.1114G=	ENSP00000378740.3:p.Gly372=
ENST00000395332.7:c.1174G=	ENSP00000378741.3:p.Gly392=
ENST00000450043.2:c.487G=	ENSP00000396527.2:p.Gly163=
ENST00000464970.1:n.377G=
ENST00000488343.1:n.148-317G=
ENST00000493708.5:n.655G=
NM_000048.3:c.1174G=	NP_000039.2:p.Gly392=
NM_001024943.1:c.1174G=	NP_001020114.1:p.Gly392=
NM_001024944.1:c.1114G=	NP_001020115.1:p.Gly372=
NM_001024946.1:c.1096G=	NP_001020117.1:p.Gly366=
NM_000048.4:c.1174G= MANE Select	NP_000039.2:p.Gly392=
NM_001024943.2:c.1174G=	NP_001020114.1:p.Gly392=
NM_001024944.2:c.1114G=	NP_001020115.1:p.Gly372=
NM_001024946.2:c.1096G=	NP_001020117.1:p.Gly366=