Canonical Allele Identifier: CA2210048717

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15992976C= , CM000678.2:g.15992976C=	GRCh38
NC_000016.9:g.16086833C= , CM000678.1:g.16086833C=	GRCh37
NC_000016.8:g.15994334C=	NCBI36
NG_028268.1:g.48400C=
NG_028268.2:g.48400C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.49-14840C= MANE Select	NP_004987.2:n.49-14840C=
ENST00000399410.8:c.49-14840C= MANE Select	ENSP00000382342.3:n.49-14840C=
NM_004996.3:c.49-14840C=	NP_004987.2:n.49-14840C=
ENST00000399408.6:c.-930-14840C=	ENSP00000382340.3:n.-930-14840C=
ENST00000399408.7:c.49-14840C=	ENSP00000382340.4:n.49-14840C=
ENST00000399410.7:c.49-14840C=	ENSP00000382342.3:n.49-14840C=
ENST00000572882.3:c.49-14840C=	ENSP00000461615.2:n.49-14840C=
ENST00000574224.2:n.124-14840C=
ENST00000677164.1:c.49-14840C=	ENSP00000502873.1:n.49-14840C=
ENST00000678422.1:c.49-14840C=	ENSP00000503954.1:n.49-14840C=
XM_011522498.1:c.102+724C=	XP_011520800.1:n.102+724C=
XM_011522498.2:c.102+724C=	XP_011520800.1:n.102+724C=
XM_017023237.1:c.102+724C=	XP_016878726.1:n.102+724C=
XM_017023238.1:c.102+724C=	XP_016878727.1:n.102+724C=
XM_017023239.1:c.102+724C=	XP_016878728.1:n.102+724C=
XM_017023240.1:c.102+724C=	XP_016878729.1:n.102+724C=
XM_017023241.1:c.102+724C=	XP_016878730.1:n.102+724C=
XM_017023242.1:c.102+724C=	XP_016878731.1:n.102+724C=
XM_017023243.2:c.102+724C=	XP_016878732.1:n.102+724C=