Canonical Allele Identifier: CA2210060905

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016516T= , CM000678.2:g.16016516T=	GRCh38
NC_000016.9:g.16110373T= , CM000678.1:g.16110373T=	GRCh37
NC_000016.8:g.16017874T=	NCBI36
NG_028268.1:g.71940T=
NG_028268.2:g.71940T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.510T=	ENSP00000382340.4:p.Phe170=
ENST00000399410.8:c.510T= MANE Select	ENSP00000382342.3:p.Phe170=
ENST00000572882.3:c.510T=	ENSP00000461615.2:p.Phe170=
ENST00000574224.2:n.585T=
ENST00000677164.1:c.489+1888T=	ENSP00000502873.1:n.489+1888T=
ENST00000678422.1:c.510T=	ENSP00000503954.1:p.Phe170=
ENST00000679043.1:n.462T=
ENST00000399408.6:c.-469T=	ENSP00000382340.3:n.-469T=
ENST00000399410.7:c.510T=	ENSP00000382342.3:p.Phe170=
ENST00000572882.2:c.205T=
ENST00000574224.1:n.110T=
NM_004996.3:c.510T=	NP_004987.2:p.Phe170=
XM_011522497.1:c.486T=	XP_011520799.1:p.Phe162=
XM_011522498.1:c.564T=	XP_011520800.1:p.Phe188=
XM_011522498.2:c.564T=	XP_011520800.1:p.Phe188=
XM_017023237.1:c.564T=	XP_016878726.1:p.Phe188=
XM_017023238.1:c.543+1888T=	XP_016878727.1:n.543+1888T=
XM_017023239.1:c.426T=	XP_016878728.1:p.Phe142=
XM_017023240.1:c.564T=	XP_016878729.1:p.Phe188=
XM_017023241.1:c.405+6615T=	XP_016878730.1:n.405+6615T=
XM_017023242.1:c.564T=	XP_016878731.1:p.Phe188=
XM_017023243.2:c.564T=	XP_016878732.1:p.Phe188=
NM_004996.4:c.510T= MANE Select	NP_004987.2:p.Phe170=