Canonical Allele Identifier: CA2548876533

Gene: ABCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16142067_16142068insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC , CM000678.2:g.16142067_16142068insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	GRCh38
NC_000016.9:g.16235924_16235925insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC , CM000678.1:g.16235924_16235925insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	GRCh37
NC_000016.8:g.16143425_16143426insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	NCBI36
NG_028268.1:g.197491_197492insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC
NG_028268.2:g.197491_197492insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000399408.7:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	ENSP00000382340.4:n.*786_*787insCCCCCCCCC...
ENST00000399410.8:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC MANE Select	ENSP00000382342.3:n.*786_*787insCCCCCCCCC...
ENST00000572882.3:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	ENSP00000461615.2:n.*786_*787insCCCCCCCCC...
ENST00000676806.1:n.2108_2109insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC
ENST00000677164.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	ENSP00000502873.1:n.*786_*787insCCCCCCCCC...
ENST00000678422.1:c.*2479_*2480insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	ENSP00000503954.1:n.*2479_*2480insCCCCCCC...
ENST00000399408.6:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	ENSP00000382340.3:n.*786_*787insCCCCCCCCC...
ENST00000399410.7:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	ENSP00000382342.3:n.*786_*787insCCCCCCCCC...
NM_004996.3:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	NP_004987.2:n.*786_*787insCCCCCCCCCCCCCCC...
XM_011522497.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_011520799.1:n.*786_*787insCCCCCCCCCCCC...
XM_011522498.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_011520800.1:n.*786_*787insCCCCCCCCCCCC...
XM_011522498.2:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_011520800.1:n.*786_*787insCCCCCCCCCCCC...
XM_017023237.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_016878726.1:n.*786_*787insCCCCCCCCCCCC...
XM_017023238.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_016878727.1:n.*786_*787insCCCCCCCCCCCC...
XM_017023239.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_016878728.1:n.*786_*787insCCCCCCCCCCCC...
XM_017023240.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_016878729.1:n.*786_*787insCCCCCCCCCCCC...
XM_017023241.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_016878730.1:n.*786_*787insCCCCCCCCCCCC...
XM_017023242.1:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC	XP_016878731.1:n.*786_*787insCCCCCCCCCCCC...
NM_004996.4:c.*786_*787insCCCCCCCCCCCCCCCCCCCCCCGGGCTTCCC MANE Select	NP_004987.2:n.*786_*787insCCCCCCCCCCCCCCC...