Canonical Allele Identifier: CA2210060901

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016503A= , CM000678.2:g.16016503A=	GRCh38
NC_000016.9:g.16110360A= , CM000678.1:g.16110360A=	GRCh37
NC_000016.8:g.16017861A=	NCBI36
NG_028268.1:g.71927A=
NG_028268.2:g.71927A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.497A=	ENSP00000382340.4:p.Gln166=
ENST00000399410.8:c.497A= MANE Select	ENSP00000382342.3:p.Gln166=
ENST00000572882.3:c.497A=	ENSP00000461615.2:p.Gln166=
ENST00000574224.2:n.572A=
ENST00000677164.1:c.489+1875A=	ENSP00000502873.1:n.489+1875A=
ENST00000678422.1:c.497A=	ENSP00000503954.1:p.Gln166=
ENST00000679043.1:n.449A=
ENST00000399408.6:c.-482A=	ENSP00000382340.3:n.-482A=
ENST00000399410.7:c.497A=	ENSP00000382342.3:p.Gln166=
ENST00000572882.2:c.192A=
ENST00000574224.1:n.97A=
NM_004996.3:c.497A=	NP_004987.2:p.Gln166=
XM_011522497.1:c.473A=	XP_011520799.1:p.Gln158=
XM_011522498.1:c.551A=	XP_011520800.1:p.Gln184=
XM_011522498.2:c.551A=	XP_011520800.1:p.Gln184=
XM_017023237.1:c.551A=	XP_016878726.1:p.Gln184=
XM_017023238.1:c.543+1875A=	XP_016878727.1:n.543+1875A=
XM_017023239.1:c.413A=	XP_016878728.1:p.Gln138=
XM_017023240.1:c.551A=	XP_016878729.1:p.Gln184=
XM_017023241.1:c.405+6602A=	XP_016878730.1:n.405+6602A=
XM_017023242.1:c.551A=	XP_016878731.1:p.Gln184=
XM_017023243.2:c.551A=	XP_016878732.1:p.Gln184=
NM_004996.4:c.497A= MANE Select	NP_004987.2:p.Gln166=