Canonical Allele Identifier: CA2210109454

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16111468G= , CM000678.2:g.16111468G=	GRCh38
NC_000016.9:g.16205325G= , CM000678.1:g.16205325G=	GRCh37
NC_000016.8:g.16112826G=	NCBI36
NG_028268.1:g.166892G=
NG_028268.2:g.166892G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.2965G= MANE Select	NP_004987.2:p.Ala989=
ENST00000399410.8:c.2965G= MANE Select	ENSP00000382342.3:p.Ala989=
NM_004996.3:c.2965G=	NP_004987.2:p.Ala989=
ENST00000399408.6:c.2017G=	ENSP00000382340.3:p.Ala673=
ENST00000399408.7:c.2995G=	ENSP00000382340.4:p.Ala999=
ENST00000399410.7:c.2965G=	ENSP00000382342.3:p.Ala989=
ENST00000572053.5:c.326G=	ENSP00000459693.1:n.326G=
ENST00000572882.2:c.2690G=
ENST00000572882.3:c.2788G=	ENSP00000461615.2:p.Ala930=
ENST00000574761.1:n.442G=
ENST00000677164.1:c.2494G=	ENSP00000502873.1:p.Ala832=
ENST00000678422.1:c.*257G=	ENSP00000503954.1:n.*257G=
XM_011522497.1:c.2941G=	XP_011520799.1:p.Ala981=
XM_011522498.1:c.2872G=	XP_011520800.1:p.Ala958=
XM_011522498.2:c.2872G=	XP_011520800.1:p.Ala958=
XM_017023237.1:c.3019G=	XP_016878726.1:p.Ala1007=
XM_017023238.1:c.2893G=	XP_016878727.1:p.Ala965=
XM_017023239.1:c.2881G=	XP_016878728.1:p.Ala961=
XM_017023240.1:c.2842G=	XP_016878729.1:p.Ala948=
XM_017023241.1:c.2755G=	XP_016878730.1:p.Ala919=
XM_017023242.1:c.2674G=	XP_016878731.1:p.Ala892=