Canonical Allele Identifier: CA2210060796

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016299G= , CM000678.2:g.16016299G=	GRCh38
NC_000016.9:g.16110156G= , CM000678.1:g.16110156G=	GRCh37
NC_000016.8:g.16017657G=	NCBI36
NG_028268.1:g.71723G=
NG_028268.2:g.71723G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.490-197G= MANE Select	NP_004987.2:n.490-197G=
ENST00000399410.8:c.490-197G= MANE Select	ENSP00000382342.3:n.490-197G=
NM_004996.3:c.490-197G=	NP_004987.2:n.490-197G=
ENST00000399408.6:c.-489-197G=	ENSP00000382340.3:n.-489-197G=
ENST00000399408.7:c.490-197G=	ENSP00000382340.4:n.490-197G=
ENST00000399410.7:c.490-197G=	ENSP00000382342.3:n.490-197G=
ENST00000572882.2:c.185-197G=
ENST00000572882.3:c.490-197G=	ENSP00000461615.2:n.490-197G=
ENST00000574224.1:n.90-197G=
ENST00000574224.2:n.565-197G=
ENST00000677164.1:c.489+1671G=	ENSP00000502873.1:n.489+1671G=
ENST00000678422.1:c.490-197G=	ENSP00000503954.1:n.490-197G=
ENST00000679043.1:n.442-197G=
XM_011522497.1:c.466-197G=	XP_011520799.1:n.466-197G=
XM_011522498.1:c.544-197G=	XP_011520800.1:n.544-197G=
XM_011522498.2:c.544-197G=	XP_011520800.1:n.544-197G=
XM_017023237.1:c.544-197G=	XP_016878726.1:n.544-197G=
XM_017023238.1:c.543+1671G=	XP_016878727.1:n.543+1671G=
XM_017023239.1:c.406-197G=	XP_016878728.1:n.406-197G=
XM_017023240.1:c.544-197G=	XP_016878729.1:n.544-197G=
XM_017023241.1:c.405+6398G=	XP_016878730.1:n.405+6398G=
XM_017023242.1:c.544-197G=	XP_016878731.1:n.544-197G=
XM_017023243.2:c.544-197G=	XP_016878732.1:n.544-197G=