Canonical Allele Identifier: CA2631957089

Gene: ABCC1

Linked Data

• gnomAD v4: 16-16016403-C-CATTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016403_16016404insATTAAAAAA , CM000678.2:g.16016403_16016404insATTAAAAAA	GRCh38
NC_000016.9:g.16110260_16110261insATTAAAAAA , CM000678.1:g.16110260_16110261insATTAAAAAA	GRCh37
NC_000016.8:g.16017761_16017762insATTAAAAAA	NCBI36
NG_028268.1:g.71827_71828insATTAAAAAA
NG_028268.2:g.71827_71828insATTAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.490-93_490-92insATTAAAAAA	ENSP00000382340.4:n.490-93_490-92insATTAAAAAA
ENST00000399410.8:c.490-93_490-92insATTAAAAAA MANE Select	ENSP00000382342.3:n.490-93_490-92insATTAAAAAA
ENST00000572882.3:c.490-93_490-92insATTAAAAAA	ENSP00000461615.2:n.490-93_490-92insATTAAAAAA
ENST00000574224.2:n.565-93_565-92insATTAAAAAA
ENST00000677164.1:c.489+1775_489+1776insATTAAAAAA	ENSP00000502873.1:n.489+1775_489+1776insATTAAAAAA
ENST00000678422.1:c.490-93_490-92insATTAAAAAA	ENSP00000503954.1:n.490-93_490-92insATTAAAAAA
ENST00000679043.1:n.442-93_442-92insATTAAAAAA
ENST00000399408.6:c.-489-93_-489-92insATTAAAAAA	ENSP00000382340.3:n.-489-93_-489-92insATTAAAAAA
ENST00000399410.7:c.490-93_490-92insATTAAAAAA	ENSP00000382342.3:n.490-93_490-92insATTAAAAAA
ENST00000572882.2:c.185-93_185-92insATTAAAAAA
ENST00000574224.1:n.90-93_90-92insATTAAAAAA
NM_004996.3:c.490-93_490-92insATTAAAAAA	NP_004987.2:n.490-93_490-92insATTAAAAAA
XM_011522497.1:c.466-93_466-92insATTAAAAAA	XP_011520799.1:n.466-93_466-92insATTAAAAAA
XM_011522498.1:c.544-93_544-92insATTAAAAAA	XP_011520800.1:n.544-93_544-92insATTAAAAAA
XM_011522498.2:c.544-93_544-92insATTAAAAAA	XP_011520800.1:n.544-93_544-92insATTAAAAAA
XM_017023237.1:c.544-93_544-92insATTAAAAAA	XP_016878726.1:n.544-93_544-92insATTAAAAAA
XM_017023238.1:c.543+1775_543+1776insATTAAAAAA	XP_016878727.1:n.543+1775_543+1776insATTAAAAAA
XM_017023239.1:c.406-93_406-92insATTAAAAAA	XP_016878728.1:n.406-93_406-92insATTAAAAAA
XM_017023240.1:c.544-93_544-92insATTAAAAAA	XP_016878729.1:n.544-93_544-92insATTAAAAAA
XM_017023241.1:c.405+6502_405+6503insATTAAAAAA	XP_016878730.1:n.405+6502_405+6503insATTAAAAAA
XM_017023242.1:c.544-93_544-92insATTAAAAAA	XP_016878731.1:n.544-93_544-92insATTAAAAAA
XM_017023243.2:c.544-93_544-92insATTAAAAAA	XP_016878732.1:n.544-93_544-92insATTAAAAAA
NM_004996.4:c.490-93_490-92insATTAAAAAA MANE Select	NP_004987.2:n.490-93_490-92insATTAAAAAA