Canonical Allele Identifier: CA3000195472

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16016412del , CM000678.2:g.16016412del	GRCh38
NC_000016.9:g.16110269del , CM000678.1:g.16110269del	GRCh37
NC_000016.8:g.16017770del	NCBI36
NG_028268.1:g.71836del
NG_028268.2:g.71836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.490-84del	ENSP00000382340.4:n.490-84del
ENST00000399410.8:c.490-84del MANE Select	ENSP00000382342.3:n.490-84del
ENST00000572882.3:c.490-84del	ENSP00000461615.2:n.490-84del
ENST00000574224.2:n.565-84del
ENST00000677164.1:c.489+1784del	ENSP00000502873.1:n.489+1784del
ENST00000678422.1:c.490-84del	ENSP00000503954.1:n.490-84del
ENST00000679043.1:n.442-84del
ENST00000399408.6:c.-489-84del	ENSP00000382340.3:n.-489-84del
ENST00000399410.7:c.490-84del	ENSP00000382342.3:n.490-84del
ENST00000572882.2:c.185-84del
ENST00000574224.1:n.90-84del
NM_004996.3:c.490-84del	NP_004987.2:n.490-84del
XM_011522497.1:c.466-84del	XP_011520799.1:n.466-84del
XM_011522498.1:c.544-84del	XP_011520800.1:n.544-84del
XM_011522498.2:c.544-84del	XP_011520800.1:n.544-84del
XM_017023237.1:c.544-84del	XP_016878726.1:n.544-84del
XM_017023238.1:c.543+1784del	XP_016878727.1:n.543+1784del
XM_017023239.1:c.406-84del	XP_016878728.1:n.406-84del
XM_017023240.1:c.544-84del	XP_016878729.1:n.544-84del
XM_017023241.1:c.405+6511del	XP_016878730.1:n.405+6511del
XM_017023242.1:c.544-84del	XP_016878731.1:n.544-84del
XM_017023243.2:c.544-84del	XP_016878732.1:n.544-84del
NM_004996.4:c.490-84del MANE Select	NP_004987.2:n.490-84del