Canonical Allele Identifier: CA2210060913

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016530T= , CM000678.2:g.16016530T=	GRCh38
NC_000016.9:g.16110387T= , CM000678.1:g.16110387T=	GRCh37
NC_000016.8:g.16017888T=	NCBI36
NG_028268.1:g.71954T=
NG_028268.2:g.71954T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.524T=	ENSP00000382340.4:p.Phe175=
ENST00000399410.8:c.524T= MANE Select	ENSP00000382342.3:p.Phe175=
ENST00000572882.3:c.524T=	ENSP00000461615.2:p.Phe175=
ENST00000574224.2:n.599T=
ENST00000677164.1:c.489+1902T=	ENSP00000502873.1:n.489+1902T=
ENST00000678422.1:c.524T=	ENSP00000503954.1:p.Phe175=
ENST00000679043.1:n.476T=
ENST00000399408.6:c.-455T=	ENSP00000382340.3:n.-455T=
ENST00000399410.7:c.524T=	ENSP00000382342.3:p.Phe175=
ENST00000572882.2:c.219T=
ENST00000574224.1:n.124T=
NM_004996.3:c.524T=	NP_004987.2:p.Phe175=
XM_011522497.1:c.500T=	XP_011520799.1:p.Phe167=
XM_011522498.1:c.578T=	XP_011520800.1:p.Phe193=
XM_011522498.2:c.578T=	XP_011520800.1:p.Phe193=
XM_017023237.1:c.578T=	XP_016878726.1:p.Phe193=
XM_017023238.1:c.543+1902T=	XP_016878727.1:n.543+1902T=
XM_017023239.1:c.440T=	XP_016878728.1:p.Phe147=
XM_017023240.1:c.578T=	XP_016878729.1:p.Phe193=
XM_017023241.1:c.405+6629T=	XP_016878730.1:n.405+6629T=
XM_017023242.1:c.578T=	XP_016878731.1:p.Phe193=
XM_017023243.2:c.578T=	XP_016878732.1:p.Phe193=
NM_004996.4:c.524T= MANE Select	NP_004987.2:p.Phe175=