Canonical Allele Identifier: CA2610496237
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830315_99830316insACTA , CM000672.2:g.99830315_99830316insACTA GRCh38
NC_000010.10:g.101590072_101590073insACTA , CM000672.1:g.101590072_101590073insACTA GRCh37
NC_000010.9:g.101580062_101580063insACTA NCBI36
NG_011798.1:g.52610_52611insACTA
NG_011798.2:g.52718_52719insACTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2629_2630insACTA MANE Select ENSP00000497274.1:p.Gly877AspfsTer2
ENST00000370449.8:c.2629_2630insACTA ENSP00000359478.4:p.Gly877AspfsTer2
NM_000392.4:c.2629_2630insACTA NP_000383.1:p.Gly877AspfsTer2
XM_006717630.2:c.1933_1934insACTA XP_006717693.1:p.Gly645AspfsTer2
XM_006717631.2:c.*56_*57insACTA XP_006717694.1:n.*56_*57insACTA
XM_011539291.1:c.2629_2630insACTA XP_011537593.1:p.Gly877AspfsTer2
XR_945604.1:n.2818_2819insACTA
XR_945605.1:n.2820_2821insACTA
NM_000392.5:c.2629_2630insACTA MANE Select NP_000383.2:p.Gly877AspfsTer2
XM_006717630.3:c.1933_1934insACTA XP_006717693.1:p.Gly645AspfsTer2
XM_006717631.4:c.*56_*57insACTA XP_006717694.1:n.*56_*57insACTA
XM_011539291.3:c.2629_2630insACTA XP_011537593.1:p.Gly877AspfsTer2
XR_945604.3:n.2872_2873insACTA
XR_945605.3:n.2872_2873insACTA