Canonical Allele Identifier: CA2210095475

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16079380T= , CM000678.2:g.16079380T=	GRCh38
NC_000016.9:g.16173237T= , CM000678.1:g.16173237T=	GRCh37
NC_000016.8:g.16080738T=	NCBI36
NG_028268.1:g.134804T=
NG_028268.2:g.134804T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.2017T=	ENSP00000382340.4:p.Leu673=
ENST00000399410.8:c.2017T= MANE Select	ENSP00000382342.3:p.Leu673=
ENST00000572882.3:c.2017T=	ENSP00000461615.2:p.Leu673=
ENST00000677164.1:c.1891T=	ENSP00000502873.1:p.Leu631=
ENST00000678422.1:c.2017T=	ENSP00000503954.1:p.Leu673=
ENST00000399408.6:c.1039T=	ENSP00000382340.3:p.Leu347=
ENST00000399410.7:c.2017T=	ENSP00000382342.3:p.Leu673=
ENST00000572882.2:c.1712T=
ENST00000575422.5:n.257T=
NM_004996.3:c.2017T=	NP_004987.2:p.Leu673=
XM_011522497.1:c.1993T=	XP_011520799.1:p.Leu665=
XM_011522498.1:c.1924T=	XP_011520800.1:p.Leu642=
XM_011522498.2:c.1924T=	XP_011520800.1:p.Leu642=
XM_017023237.1:c.2071T=	XP_016878726.1:p.Leu691=
XM_017023238.1:c.1945T=	XP_016878727.1:p.Leu649=
XM_017023239.1:c.1933T=	XP_016878728.1:p.Leu645=
XM_017023240.1:c.2071T=	XP_016878729.1:p.Leu691=
XM_017023241.1:c.1807T=	XP_016878730.1:p.Leu603=
XM_017023242.1:c.2071T=	XP_016878731.1:p.Leu691=
XM_017023243.2:c.2071T=	XP_016878732.1:p.Leu691=
NM_004996.4:c.2017T= MANE Select	NP_004987.2:p.Leu673=