Canonical Allele Identifier: CA1931514535
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845966_99845967delinsTG , CM000672.2:g.99845966_99845967delinsTG GRCh38
NC_000010.10:g.101605723_101605724delinsTG , CM000672.1:g.101605723_101605724delinsTG GRCh37
NC_000010.9:g.101595713_101595714delinsTG NCBI36
NG_011798.1:g.68261_68262delinsTG
NG_011798.2:g.68369_68370delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4146+184_4146+185delinsTG MANE Select ENSP00000497274.1:n.4146+184_4146+185deli...
ENST00000648523.1:c.34+184_34+185delinsTG
ENST00000649459.1:n.494+184_494+185delinsTG
ENST00000370449.8:c.4146+184_4146+185delinsTG ENSP00000359478.4:n.4146+184_4146+185deli...
NM_000392.4:c.4146+184_4146+185delinsTG NP_000383.1:n.4146+184_4146+185delinsTG
XM_006717630.2:c.3450+184_3450+185delinsTG XP_006717693.1:n.3450+184_3450+185delinsT...
XR_945604.1:n.4276+184_4276+185delinsTG
XR_945605.1:n.4210+184_4210+185delinsTG
NM_000392.5:c.4146+184_4146+185delinsTG MANE Select NP_000383.2:n.4146+184_4146+185delinsTG
XM_006717630.3:c.3450+184_3450+185delinsTG XP_006717693.1:n.3450+184_3450+185delinsT...
XR_945604.3:n.4330+184_4330+185delinsTG
XR_945605.3:n.4262+184_4262+185delinsTG