Canonical Allele Identifier: CA656777713

Gene: ABCC1

Linked Data

• COSMIC: COSN17578833 ; COSN21001603

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16142409_16142410insT , CM000678.2:g.16142409_16142410insT	GRCh38
NC_000016.9:g.16236266_16236267insT , CM000678.1:g.16236266_16236267insT	GRCh37
NC_000016.8:g.16143767_16143768insT	NCBI36
NG_028268.1:g.197833_197834insT
NG_028268.2:g.197833_197834insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399408.7:c.*1128_*1129insT	ENSP00000382340.4:n.*1128_*1129insT
ENST00000399410.8:c.*1128_*1129insT MANE Select	ENSP00000382342.3:n.*1128_*1129insT
ENST00000572882.3:c.*1128_*1129insT	ENSP00000461615.2:n.*1128_*1129insT
ENST00000676806.1:n.2450_2451insT
ENST00000677164.1:c.*1128_*1129insT	ENSP00000502873.1:n.*1128_*1129insT
ENST00000678422.1:c.*2821_*2822insT	ENSP00000503954.1:n.*2821_*2822insT
ENST00000399408.6:c.*1128_*1129insT	ENSP00000382340.3:n.*1128_*1129insT
ENST00000399410.7:c.*1128_*1129insT	ENSP00000382342.3:n.*1128_*1129insT
NM_004996.3:c.*1128_*1129insT	NP_004987.2:n.*1128_*1129insT
XM_011522497.1:c.*1128_*1129insT	XP_011520799.1:n.*1128_*1129insT
XM_011522498.1:c.*1128_*1129insT	XP_011520800.1:n.*1128_*1129insT
XM_011522498.2:c.*1128_*1129insT	XP_011520800.1:n.*1128_*1129insT
XM_017023237.1:c.*1128_*1129insT	XP_016878726.1:n.*1128_*1129insT
XM_017023238.1:c.*1128_*1129insT	XP_016878727.1:n.*1128_*1129insT
XM_017023239.1:c.*1128_*1129insT	XP_016878728.1:n.*1128_*1129insT
XM_017023240.1:c.*1128_*1129insT	XP_016878729.1:n.*1128_*1129insT
XM_017023241.1:c.*1128_*1129insT	XP_016878730.1:n.*1128_*1129insT
XM_017023242.1:c.*1128_*1129insT	XP_016878731.1:n.*1128_*1129insT
NM_004996.4:c.*1128_*1129insT MANE Select	NP_004987.2:n.*1128_*1129insT