Canonical Allele Identifier: CA14355639

Gene: ABCC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016244C>T , CM000678.2:g.16016244C>T	GRCh38
NC_000016.9:g.16110101C>T , CM000678.1:g.16110101C>T	GRCh37
NC_000016.8:g.16017602C>T	NCBI36
NG_028268.1:g.71668C>T
NG_028268.2:g.71668C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.490-252C>T	ENSP00000382340.4:n.490-252C>T
ENST00000399410.8:c.490-252C>T MANE Select	ENSP00000382342.3:n.490-252C>T
ENST00000572882.3:c.490-252C>T	ENSP00000461615.2:n.490-252C>T
ENST00000574224.2:n.565-252C>T
ENST00000677164.1:c.489+1616C>T	ENSP00000502873.1:n.489+1616C>T
ENST00000678422.1:c.490-252C>T	ENSP00000503954.1:n.490-252C>T
ENST00000679043.1:n.442-252C>T
ENST00000399408.6:c.-489-252C>T	ENSP00000382340.3:n.-489-252C>T
ENST00000399410.7:c.490-252C>T	ENSP00000382342.3:n.490-252C>T
ENST00000572882.2:c.185-252C>T
ENST00000574224.1:n.90-252C>T
NM_004996.3:c.490-252C>T	NP_004987.2:n.490-252C>T
XM_011522497.1:c.466-252C>T	XP_011520799.1:n.466-252C>T
XM_011522498.1:c.544-252C>T	XP_011520800.1:n.544-252C>T
XM_011522498.2:c.544-252C>T	XP_011520800.1:n.544-252C>T
XM_017023237.1:c.544-252C>T	XP_016878726.1:n.544-252C>T
XM_017023238.1:c.543+1616C>T	XP_016878727.1:n.543+1616C>T
XM_017023239.1:c.406-252C>T	XP_016878728.1:n.406-252C>T
XM_017023240.1:c.544-252C>T	XP_016878729.1:n.544-252C>T
XM_017023241.1:c.405+6343C>T	XP_016878730.1:n.405+6343C>T
XM_017023242.1:c.544-252C>T	XP_016878731.1:n.544-252C>T
XM_017023243.2:c.544-252C>T	XP_016878732.1:n.544-252C>T
NM_004996.4:c.490-252C>T MANE Select	NP_004987.2:n.490-252C>T