Canonical Allele Identifier: CA2210060794

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016298T= , CM000678.2:g.16016298T=	GRCh38
NC_000016.9:g.16110155T= , CM000678.1:g.16110155T=	GRCh37
NC_000016.8:g.16017656T=	NCBI36
NG_028268.1:g.71722T=
NG_028268.2:g.71722T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.490-198T= MANE Select	NP_004987.2:n.490-198T=
ENST00000399410.8:c.490-198T= MANE Select	ENSP00000382342.3:n.490-198T=
NM_004996.3:c.490-198T=	NP_004987.2:n.490-198T=
ENST00000399408.6:c.-489-198T=	ENSP00000382340.3:n.-489-198T=
ENST00000399408.7:c.490-198T=	ENSP00000382340.4:n.490-198T=
ENST00000399410.7:c.490-198T=	ENSP00000382342.3:n.490-198T=
ENST00000572882.2:c.185-198T=
ENST00000572882.3:c.490-198T=	ENSP00000461615.2:n.490-198T=
ENST00000574224.1:n.90-198T=
ENST00000574224.2:n.565-198T=
ENST00000677164.1:c.489+1670T=	ENSP00000502873.1:n.489+1670T=
ENST00000678422.1:c.490-198T=	ENSP00000503954.1:n.490-198T=
ENST00000679043.1:n.442-198T=
XM_011522497.1:c.466-198T=	XP_011520799.1:n.466-198T=
XM_011522498.1:c.544-198T=	XP_011520800.1:n.544-198T=
XM_011522498.2:c.544-198T=	XP_011520800.1:n.544-198T=
XM_017023237.1:c.544-198T=	XP_016878726.1:n.544-198T=
XM_017023238.1:c.543+1670T=	XP_016878727.1:n.543+1670T=
XM_017023239.1:c.406-198T=	XP_016878728.1:n.406-198T=
XM_017023240.1:c.544-198T=	XP_016878729.1:n.544-198T=
XM_017023241.1:c.405+6397T=	XP_016878730.1:n.405+6397T=
XM_017023242.1:c.544-198T=	XP_016878731.1:n.544-198T=
XM_017023243.2:c.544-198T=	XP_016878732.1:n.544-198T=