Canonical Allele Identifier: CA2210125480

Gene: ABCC1

Linked Data

• dbSNP Id: rs2046142615

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16142061del , CM000678.2:g.16142061del	GRCh38
NC_000016.9:g.16235918del , CM000678.1:g.16235918del	GRCh37
NC_000016.8:g.16143419del	NCBI36
NG_028268.1:g.197485del
NG_028268.2:g.197485del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399408.7:c.*780del	ENSP00000382340.4:n.*780del
ENST00000399410.8:c.*780del MANE Select	ENSP00000382342.3:n.*780del
ENST00000572882.3:c.*780del	ENSP00000461615.2:n.*780del
ENST00000676806.1:n.2102del
ENST00000677164.1:c.*780del	ENSP00000502873.1:n.*780del
ENST00000678422.1:c.*2473del	ENSP00000503954.1:n.*2473del
ENST00000399408.6:c.*780del	ENSP00000382340.3:n.*780del
ENST00000399410.7:c.*780del	ENSP00000382342.3:n.*780del
NM_004996.3:c.*780del	NP_004987.2:n.*780del
XM_011522497.1:c.*780del	XP_011520799.1:n.*780del
XM_011522498.1:c.*780del	XP_011520800.1:n.*780del
XM_011522498.2:c.*780del	XP_011520800.1:n.*780del
XM_017023237.1:c.*780del	XP_016878726.1:n.*780del
XM_017023238.1:c.*780del	XP_016878727.1:n.*780del
XM_017023239.1:c.*780del	XP_016878728.1:n.*780del
XM_017023240.1:c.*780del	XP_016878729.1:n.*780del
XM_017023241.1:c.*780del	XP_016878730.1:n.*780del
XM_017023242.1:c.*780del	XP_016878731.1:n.*780del
NM_004996.4:c.*780del MANE Select	NP_004987.2:n.*780del