Canonical Allele Identifier: CA2210089689

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16068182C= , CM000678.2:g.16068182C=	GRCh38
NC_000016.9:g.16162039C= , CM000678.1:g.16162039C=	GRCh37
NC_000016.8:g.16069540C=	NCBI36
NG_028268.1:g.123606C=
NG_028268.2:g.123606C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.1704C= MANE Select	NP_004987.2:p.Tyr568=
ENST00000399410.8:c.1704C= MANE Select	ENSP00000382342.3:p.Tyr568=
NM_004996.3:c.1704C=	NP_004987.2:p.Tyr568=
ENST00000399408.6:c.726C=	ENSP00000382340.3:p.Tyr242=
ENST00000399408.7:c.1704C=	ENSP00000382340.4:p.Tyr568=
ENST00000399410.7:c.1704C=	ENSP00000382342.3:p.Tyr568=
ENST00000572882.2:c.1399C=
ENST00000572882.3:c.1704C=	ENSP00000461615.2:p.Tyr568=
ENST00000677164.1:c.1578C=	ENSP00000502873.1:p.Tyr526=
ENST00000678422.1:c.1704C=	ENSP00000503954.1:p.Tyr568=
XM_011522497.1:c.1680C=	XP_011520799.1:p.Tyr560=
XM_011522498.1:c.1732-3460C=	XP_011520800.1:n.1732-3460C=
XM_011522498.2:c.1732-3460C=	XP_011520800.1:n.1732-3460C=
XM_017023237.1:c.1758C=	XP_016878726.1:p.Tyr586=
XM_017023238.1:c.1632C=	XP_016878727.1:p.Tyr544=
XM_017023239.1:c.1620C=	XP_016878728.1:p.Tyr540=
XM_017023240.1:c.1758C=	XP_016878729.1:p.Tyr586=
XM_017023241.1:c.1494C=	XP_016878730.1:p.Tyr498=
XM_017023242.1:c.1758C=	XP_016878731.1:p.Tyr586=
XM_017023243.2:c.1758C=	XP_016878732.1:p.Tyr586=