Canonical Allele Identifier: CA493794551

Gene: ABCC1

Linked Data

• MyVariant Identifiers: chr16:g.16110382C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016525C>A , CM000678.2:g.16016525C>A	GRCh38
NC_000016.9:g.16110382C>A , CM000678.1:g.16110382C>A	GRCh37
NC_000016.8:g.16017883C>A	NCBI36
NG_028268.1:g.71949C>A
NG_028268.2:g.71949C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.519C>A	ENSP00000382340.4:p.Ile173=
ENST00000399410.8:c.519C>A MANE Select	ENSP00000382342.3:p.Ile173=
ENST00000572882.3:c.519C>A	ENSP00000461615.2:p.Ile173=
ENST00000574224.2:n.594C>A
ENST00000677164.1:c.489+1897C>A	ENSP00000502873.1:n.489+1897C>A
ENST00000678422.1:c.519C>A	ENSP00000503954.1:p.Ile173=
ENST00000679043.1:n.471C>A
ENST00000399408.6:c.-460C>A	ENSP00000382340.3:n.-460C>A
ENST00000399410.7:c.519C>A	ENSP00000382342.3:p.Ile173=
ENST00000572882.2:c.214C>A
ENST00000574224.1:n.119C>A
NM_004996.3:c.519C>A	NP_004987.2:p.Ile173=
XM_011522497.1:c.495C>A	XP_011520799.1:p.Ile165=
XM_011522498.1:c.573C>A	XP_011520800.1:p.Ile191=
XM_011522498.2:c.573C>A	XP_011520800.1:p.Ile191=
XM_017023237.1:c.573C>A	XP_016878726.1:p.Ile191=
XM_017023238.1:c.543+1897C>A	XP_016878727.1:n.543+1897C>A
XM_017023239.1:c.435C>A	XP_016878728.1:p.Ile145=
XM_017023240.1:c.573C>A	XP_016878729.1:p.Ile191=
XM_017023241.1:c.405+6624C>A	XP_016878730.1:n.405+6624C>A
XM_017023242.1:c.573C>A	XP_016878731.1:p.Ile191=
XM_017023243.2:c.573C>A	XP_016878732.1:p.Ile191=
NM_004996.4:c.519C>A MANE Select	NP_004987.2:p.Ile173=