Canonical Allele Identifier: CA1515641691

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437337T= , CM000666.2:g.177437337T=	GRCh38
NC_000004.11:g.178358491T= , CM000666.1:g.178358491T=	GRCh37
NC_000004.10:g.178595485T=	NCBI36
NG_011845.2:g.10167A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.622+68A= MANE Select	ENSP00000264595.2:n.622+68A=
ENST00000264595.6:c.622+68A=	ENSP00000264595.2:n.622+68A=
ENST00000502310.5:c.277+68A=	ENSP00000423798.1:n.277+68A=
ENST00000506853.5:n.656+68A=
ENST00000510635.1:c.318+68A=
ENST00000510955.5:n.611A=
NM_000027.3:c.622+68A=	NP_000018.2:n.622+68A=
NM_001171988.1:c.622+68A=	NP_001165459.1:n.622+68A=
NR_033655.1:n.750+68A=
XM_006714123.2:c.622+68A=	XP_006714186.1:n.622+68A=
XR_001741155.2:n.716+68A=
NM_000027.4:c.622+68A= MANE Select	NP_000018.2:n.622+68A=
NM_001171988.2:c.622+68A=	NP_001165459.1:n.622+68A=
NR_033655.2:n.684+68A=