Canonical Allele Identifier: CA2264139550

Gene: ABCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50676062C= , CM000679.2:g.50676062C=	GRCh38
NC_000017.10:g.48753423C= , CM000679.1:g.48753423C=	GRCh37
NC_000017.9:g.46108422C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003786.4:c.3039C= MANE Select	NP_003777.2:p.Gly1013=
ENST00000285238.13:c.3039C= MANE Select	ENSP00000285238.8:p.Gly1013=
NM_003786.3:c.3039C=	NP_003777.2:p.Gly1013=
ENST00000285238.12:c.3039C=	ENSP00000285238.8:p.Gly1013=
ENST00000502426.5:c.*1561C=	ENSP00000427073.1:n.*1561C=
ENST00000505699.5:c.3039C=	ENSP00000427521.1:p.Gly1013=
ENST00000510633.5:c.828C=	ENSP00000422058.1:n.828C=
ENST00000510891.1:n.675C=
ENST00000513745.1:c.484C=
XM_005257763.2:c.2847C=	XP_005257820.1:p.Gly949=
XM_005257763.3:c.2847C=	XP_005257820.1:p.Gly949=
XM_011525422.1:c.2952C=	XP_011523724.1:p.Gly984=
XM_011525422.2:c.2952C=	XP_011523724.1:p.Gly984=
XM_011525423.1:c.3144C=	XP_011523725.1:p.Gly1048=
XM_011525424.1:c.2364C=	XP_011523726.1:p.Gly788=
XM_011525424.2:c.2364C=	XP_011523726.1:p.Gly788=
XM_011525425.1:c.2313C=	XP_011523727.1:p.Gly771=
XM_011525425.2:c.2313C=	XP_011523727.1:p.Gly771=
XM_017025265.2:c.2313C=	XP_016880754.1:p.Gly771=
XM_017025266.1:c.3144C=	XP_016880755.1:p.Gly1048=
XR_001752674.1:n.3238C=
XR_934586.1:n.3237C=
XR_934586.3:n.3238C=