Canonical Allele Identifier: CA1713941289

Gene: ASL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66083187G= , CM000669.2:g.66083187G=	GRCh38
NC_000007.13:g.65548174G= , CM000669.1:g.65548174G=	GRCh37
NC_000007.12:g.65185609G=	NCBI36
NG_009288.1:g.12399G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304874.14:c.446+13G= MANE Select	ENSP00000307188.9:n.446+13G=
ENST00000362000.10:c.251+13G=	ENSP00000354710.6:n.251+13G=
ENST00000380839.9:c.446+13G=	ENSP00000370219.4:n.446+13G=
ENST00000395331.4:c.446+13G=	ENSP00000378740.3:n.446+13G=
ENST00000395332.8:c.446+13G=	ENSP00000378741.3:n.446+13G=
ENST00000671817.1:c.446+13G=	ENSP00000500462.1:n.446+13G=
ENST00000672498.1:c.446+13G=	ENSP00000500227.1:n.446+13G=
ENST00000672586.1:n.351+13G=
ENST00000672676.1:n.616+13G=
ENST00000673149.1:n.258+13G=
ENST00000673350.1:n.694+13G=
ENST00000673518.1:c.446+13G=	ENSP00000499889.1:n.446+13G=
ENST00000673594.1:n.295+13G=
ENST00000304874.13:c.446+13G=	ENSP00000307188.9:n.446+13G=
ENST00000362000.9:c.251+13G=	ENSP00000354710.5:n.251+13G=
ENST00000380839.8:c.446+13G=	ENSP00000370219.4:n.446+13G=
ENST00000395331.3:c.446+13G=	ENSP00000378740.3:n.446+13G=
ENST00000395332.7:c.446+13G=	ENSP00000378741.3:n.446+13G=
ENST00000487982.5:n.512+13G=
ENST00000496336.1:n.840G=
NM_000048.3:c.446+13G=	NP_000039.2:n.446+13G=
NM_001024943.1:c.446+13G=	NP_001020114.1:n.446+13G=
NM_001024944.1:c.446+13G=	NP_001020115.1:n.446+13G=
NM_001024946.1:c.446+13G=	NP_001020117.1:n.446+13G=
NM_000048.4:c.446+13G= MANE Select	NP_000039.2:n.446+13G=
NM_001024943.2:c.446+13G=	NP_001020114.1:n.446+13G=
NM_001024944.2:c.446+13G=	NP_001020115.1:n.446+13G=
NM_001024946.2:c.446+13G=	NP_001020117.1:n.446+13G=