Canonical Allele Identifier: CA2210060912

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016527C= , CM000678.2:g.16016527C=	GRCh38
NC_000016.9:g.16110384C= , CM000678.1:g.16110384C=	GRCh37
NC_000016.8:g.16017885C=	NCBI36
NG_028268.1:g.71951C=
NG_028268.2:g.71951C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.521C=	ENSP00000382340.4:p.Thr174=
ENST00000399410.8:c.521C= MANE Select	ENSP00000382342.3:p.Thr174=
ENST00000572882.3:c.521C=	ENSP00000461615.2:p.Thr174=
ENST00000574224.2:n.596C=
ENST00000677164.1:c.489+1899C=	ENSP00000502873.1:n.489+1899C=
ENST00000678422.1:c.521C=	ENSP00000503954.1:p.Thr174=
ENST00000679043.1:n.473C=
ENST00000399408.6:c.-458C=	ENSP00000382340.3:n.-458C=
ENST00000399410.7:c.521C=	ENSP00000382342.3:p.Thr174=
ENST00000572882.2:c.216C=
ENST00000574224.1:n.121C=
NM_004996.3:c.521C=	NP_004987.2:p.Thr174=
XM_011522497.1:c.497C=	XP_011520799.1:p.Thr166=
XM_011522498.1:c.575C=	XP_011520800.1:p.Thr192=
XM_011522498.2:c.575C=	XP_011520800.1:p.Thr192=
XM_017023237.1:c.575C=	XP_016878726.1:p.Thr192=
XM_017023238.1:c.543+1899C=	XP_016878727.1:n.543+1899C=
XM_017023239.1:c.437C=	XP_016878728.1:p.Thr146=
XM_017023240.1:c.575C=	XP_016878729.1:p.Thr192=
XM_017023241.1:c.405+6626C=	XP_016878730.1:n.405+6626C=
XM_017023242.1:c.575C=	XP_016878731.1:p.Thr192=
XM_017023243.2:c.575C=	XP_016878732.1:p.Thr192=
NM_004996.4:c.521C= MANE Select	NP_004987.2:p.Thr174=