Canonical Allele Identifier: CA1515641968

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437500G= , CM000666.2:g.177437500G=	GRCh38
NC_000004.11:g.178358654G= , CM000666.1:g.178358654G=	GRCh37
NC_000004.10:g.178595648G=	NCBI36
NG_011845.2:g.10004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.527C= MANE Select	ENSP00000264595.2:p.Ser176=
ENST00000264595.6:c.527C=	ENSP00000264595.2:p.Ser176=
ENST00000502310.5:c.182C=	ENSP00000423798.1:p.Ser61=
ENST00000506853.5:n.561C=
ENST00000510635.1:c.223C=
ENST00000510955.5:n.448C=
NM_000027.3:c.527C=	NP_000018.2:p.Ser176=
NM_001171988.1:c.527C=	NP_001165459.1:p.Ser176=
NR_033655.1:n.655C=
XM_006714123.2:c.527C=	XP_006714186.1:p.Ser176=
XR_001741155.2:n.621C=
NM_000027.4:c.527C= MANE Select	NP_000018.2:p.Ser176=
NM_001171988.2:c.527C=	NP_001165459.1:p.Ser176=
NR_033655.2:n.589C=