Canonical Allele Identifier: CA2210095472

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16079375G= , CM000678.2:g.16079375G=	GRCh38
NC_000016.9:g.16173232G= , CM000678.1:g.16173232G=	GRCh37
NC_000016.8:g.16080733G=	NCBI36
NG_028268.1:g.134799G=
NG_028268.2:g.134799G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.2012G= MANE Select	NP_004987.2:p.Gly671=
ENST00000399410.8:c.2012G= MANE Select	ENSP00000382342.3:p.Gly671=
NM_004996.3:c.2012G=	NP_004987.2:p.Gly671=
ENST00000399408.6:c.1034G=	ENSP00000382340.3:p.Gly345=
ENST00000399408.7:c.2012G=	ENSP00000382340.4:p.Gly671=
ENST00000399410.7:c.2012G=	ENSP00000382342.3:p.Gly671=
ENST00000572882.2:c.1707G=
ENST00000572882.3:c.2012G=	ENSP00000461615.2:p.Gly671=
ENST00000575422.5:n.252G=
ENST00000677164.1:c.1886G=	ENSP00000502873.1:p.Gly629=
ENST00000678422.1:c.2012G=	ENSP00000503954.1:p.Gly671=
XM_011522497.1:c.1988G=	XP_011520799.1:p.Gly663=
XM_011522498.1:c.1919G=	XP_011520800.1:p.Gly640=
XM_011522498.2:c.1919G=	XP_011520800.1:p.Gly640=
XM_017023237.1:c.2066G=	XP_016878726.1:p.Gly689=
XM_017023238.1:c.1940G=	XP_016878727.1:p.Gly647=
XM_017023239.1:c.1928G=	XP_016878728.1:p.Gly643=
XM_017023240.1:c.2066G=	XP_016878729.1:p.Gly689=
XM_017023241.1:c.1802G=	XP_016878730.1:p.Gly601=
XM_017023242.1:c.2066G=	XP_016878731.1:p.Gly689=
XM_017023243.2:c.2066G=	XP_016878732.1:p.Gly689=