Canonical Allele Identifier: CA1931496449
Gene: ABCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836261_99836263delinsATG , CM000672.2:g.99836261_99836263delinsATG GRCh38
NC_000010.10:g.101596018_101596020delinsATG , CM000672.1:g.101596018_101596020delinsATG GRCh37
NC_000010.9:g.101586008_101586010delinsATG NCBI36
NG_011798.1:g.58556_58558delinsATG
NG_011798.2:g.58664_58666delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3585_3587delinsATG MANE Select ENSP00000497274.1:p.Lys1195=
ENST00000370449.8:c.3585_3587delinsATG ENSP00000359478.4:p.Lys1195=
NM_000392.4:c.3585_3587delinsATG NP_000383.1:p.Lys1195=
XM_006717630.2:c.2889_2891delinsATG XP_006717693.1:p.Lys963=
XR_945604.1:n.3774_3776delinsATG
XR_945605.1:n.3776_3778delinsATG
NM_000392.5:c.3585_3587delinsATG MANE Select NP_000383.2:p.Lys1195=
XM_006717630.3:c.2889_2891delinsATG XP_006717693.1:p.Lys963=
XR_945604.3:n.3828_3830delinsATG
XR_945605.3:n.3828_3830delinsATG
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