Canonical Allele Identifier: CA1931514197
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845797_99845805delinsTTACTCGGG , CM000672.2:g.99845797_99845805delinsTTACTCGGG GRCh38
NC_000010.10:g.101605554_101605562delinsTTACTCGGG , CM000672.1:g.101605554_101605562delinsTTACTCGGG GRCh37
NC_000010.9:g.101595544_101595552delinsTTACTCGGG NCBI36
NG_011798.1:g.68092_68100delinsTTACTCGGG
NG_011798.2:g.68200_68208delinsTTACTCGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+15_4146+23delinsTTACTCGGG MANE Select ENSP00000497274.1:n.4146+15_4146+23delins...
ENST00000648523.1:c.34+15_34+23delinsTTACTCGGG
ENST00000649459.1:n.494+15_494+23delinsTTACTCGGG
ENST00000370449.8:c.4146+15_4146+23delinsTTACTCGGG ENSP00000359478.4:n.4146+15_4146+23delins...
NM_000392.4:c.4146+15_4146+23delinsTTACTCGGG NP_000383.1:n.4146+15_4146+23delinsTTACTC...
XM_006717630.2:c.3450+15_3450+23delinsTTACTCGGG XP_006717693.1:n.3450+15_3450+23delinsTTA...
XR_945604.1:n.4276+15_4276+23delinsTTACTCGGG
XR_945605.1:n.4210+15_4210+23delinsTTACTCGGG
NM_000392.5:c.4146+15_4146+23delinsTTACTCGGG MANE Select NP_000383.2:n.4146+15_4146+23delinsTTACTC...
XM_006717630.3:c.3450+15_3450+23delinsTTACTCGGG XP_006717693.1:n.3450+15_3450+23delinsTTA...
XR_945604.3:n.4330+15_4330+23delinsTTACTCGGG
XR_945605.3:n.4262+15_4262+23delinsTTACTCGGG