Canonical Allele Identifier: CA2210095436

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16079291G= , CM000678.2:g.16079291G=	GRCh38
NC_000016.9:g.16173148G= , CM000678.1:g.16173148G=	GRCh37
NC_000016.8:g.16080649G=	NCBI36
NG_028268.1:g.134715G=
NG_028268.2:g.134715G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.1989-61G=	ENSP00000382340.4:n.1989-61G=
ENST00000399410.8:c.1989-61G= MANE Select	ENSP00000382342.3:n.1989-61G=
ENST00000572882.3:c.1989-61G=	ENSP00000461615.2:n.1989-61G=
ENST00000677164.1:c.1863-61G=	ENSP00000502873.1:n.1863-61G=
ENST00000678422.1:c.1989-61G=	ENSP00000503954.1:n.1989-61G=
ENST00000399408.6:c.1011-61G=	ENSP00000382340.3:n.1011-61G=
ENST00000399410.7:c.1989-61G=	ENSP00000382342.3:n.1989-61G=
ENST00000572882.2:c.1684-61G=
ENST00000575422.5:n.229-61G=
NM_004996.3:c.1989-61G=	NP_004987.2:n.1989-61G=
XM_011522497.1:c.1965-61G=	XP_011520799.1:n.1965-61G=
XM_011522498.1:c.1896-61G=	XP_011520800.1:n.1896-61G=
XM_011522498.2:c.1896-61G=	XP_011520800.1:n.1896-61G=
XM_017023237.1:c.2043-61G=	XP_016878726.1:n.2043-61G=
XM_017023238.1:c.1917-61G=	XP_016878727.1:n.1917-61G=
XM_017023239.1:c.1905-61G=	XP_016878728.1:n.1905-61G=
XM_017023240.1:c.2043-61G=	XP_016878729.1:n.2043-61G=
XM_017023241.1:c.1779-61G=	XP_016878730.1:n.1779-61G=
XM_017023242.1:c.2043-61G=	XP_016878731.1:n.2043-61G=
XM_017023243.2:c.2043-61G=	XP_016878732.1:n.2043-61G=
NM_004996.4:c.1989-61G= MANE Select	NP_004987.2:n.1989-61G=