Canonical Allele Identifier: CA278647315

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016279G>A , CM000678.2:g.16016279G>A	GRCh38
NC_000016.9:g.16110136G>A , CM000678.1:g.16110136G>A	GRCh37
NC_000016.8:g.16017637G>A	NCBI36
NG_028268.1:g.71703G>A
NG_028268.2:g.71703G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004996.4:c.490-217G>A MANE Select	NP_004987.2:n.490-217G>A
ENST00000399410.8:c.490-217G>A MANE Select	ENSP00000382342.3:n.490-217G>A
NM_004996.3:c.490-217G>A	NP_004987.2:n.490-217G>A
ENST00000399408.6:c.-489-217G>A	ENSP00000382340.3:n.-489-217G>A
ENST00000399408.7:c.490-217G>A	ENSP00000382340.4:n.490-217G>A
ENST00000399410.7:c.490-217G>A	ENSP00000382342.3:n.490-217G>A
ENST00000572882.2:c.185-217G>A
ENST00000572882.3:c.490-217G>A	ENSP00000461615.2:n.490-217G>A
ENST00000574224.1:n.90-217G>A
ENST00000574224.2:n.565-217G>A
ENST00000677164.1:c.489+1651G>A	ENSP00000502873.1:n.489+1651G>A
ENST00000678422.1:c.490-217G>A	ENSP00000503954.1:n.490-217G>A
ENST00000679043.1:n.442-217G>A
XM_011522497.1:c.466-217G>A	XP_011520799.1:n.466-217G>A
XM_011522498.1:c.544-217G>A	XP_011520800.1:n.544-217G>A
XM_011522498.2:c.544-217G>A	XP_011520800.1:n.544-217G>A
XM_017023237.1:c.544-217G>A	XP_016878726.1:n.544-217G>A
XM_017023238.1:c.543+1651G>A	XP_016878727.1:n.543+1651G>A
XM_017023239.1:c.406-217G>A	XP_016878728.1:n.406-217G>A
XM_017023240.1:c.544-217G>A	XP_016878729.1:n.544-217G>A
XM_017023241.1:c.405+6378G>A	XP_016878730.1:n.405+6378G>A
XM_017023242.1:c.544-217G>A	XP_016878731.1:n.544-217G>A
XM_017023243.2:c.544-217G>A	XP_016878732.1:n.544-217G>A