Canonical Allele Identifier: CA400261954

Gene: ABCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50669353G>A , CM000679.2:g.50669353G>A	GRCh38
NC_000017.10:g.48746714G>A , CM000679.1:g.48746714G>A	GRCh37
NC_000017.9:g.46101713G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003786.4:c.2066G>A MANE Select	NP_003777.2:p.Gly689Asp
ENST00000285238.13:c.2066G>A MANE Select	ENSP00000285238.8:p.Gly689Asp
NM_003786.3:c.2066G>A	NP_003777.2:p.Gly689Asp
ENST00000285238.12:c.2066G>A	ENSP00000285238.8:p.Gly689Asp
ENST00000502426.5:c.*588G>A	ENSP00000427073.1:n.*588G>A
ENST00000503304.1:n.217G>A
ENST00000505699.5:c.2066G>A	ENSP00000427521.1:p.Gly689Asp
XM_005257763.2:c.1874G>A	XP_005257820.1:p.Gly625Asp
XM_005257763.3:c.1874G>A	XP_005257820.1:p.Gly625Asp
XM_011525422.1:c.1979G>A	XP_011523724.1:p.Gly660Asp
XM_011525422.2:c.1979G>A	XP_011523724.1:p.Gly660Asp
XM_011525423.1:c.2171G>A	XP_011523725.1:p.Gly724Asp
XM_011525424.1:c.1391G>A	XP_011523726.1:p.Gly464Asp
XM_011525424.2:c.1391G>A	XP_011523726.1:p.Gly464Asp
XM_011525425.1:c.1340G>A	XP_011523727.1:p.Gly447Asp
XM_011525425.2:c.1340G>A	XP_011523727.1:p.Gly447Asp
XM_017025265.2:c.1340G>A	XP_016880754.1:p.Gly447Asp
XM_017025266.1:c.2171G>A	XP_016880755.1:p.Gly724Asp
XR_001752674.1:n.2265G>A
XR_934586.1:n.2264G>A
XR_934586.3:n.2265G>A