Canonical Allele Identifier: CA2610496238
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830316_99830317insGGAGTC , CM000672.2:g.99830316_99830317insGGAGTC GRCh38
NC_000010.10:g.101590073_101590074insGGAGTC , CM000672.1:g.101590073_101590074insGGAGTC GRCh37
NC_000010.9:g.101580063_101580064insGGAGTC NCBI36
NG_011798.1:g.52611_52612insGGAGTC
NG_011798.2:g.52719_52720insGGAGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2630_2631insGGAGTC MANE Select ENSP00000497274.1:p.Gly877_Ser878insGluSer
ENST00000370449.8:c.2630_2631insGGAGTC ENSP00000359478.4:p.Gly877_Ser878insGluSer
NM_000392.4:c.2630_2631insGGAGTC NP_000383.1:p.Gly877_Ser878insGluSer
XM_006717630.2:c.1934_1935insGGAGTC XP_006717693.1:p.Gly645_Ser646insGluSer
XM_006717631.2:c.*57_*58insGGAGTC XP_006717694.1:n.*57_*58insGGAGTC
XM_011539291.1:c.2630_2631insGGAGTC XP_011537593.1:p.Gly877_Ser878insGluSer
XR_945604.1:n.2819_2820insGGAGTC
XR_945605.1:n.2821_2822insGGAGTC
NM_000392.5:c.2630_2631insGGAGTC MANE Select NP_000383.2:p.Gly877_Ser878insGluSer
XM_006717630.3:c.1934_1935insGGAGTC XP_006717693.1:p.Gly645_Ser646insGluSer
XM_006717631.4:c.*57_*58insGGAGTC XP_006717694.1:n.*57_*58insGGAGTC
XM_011539291.3:c.2630_2631insGGAGTC XP_011537593.1:p.Gly877_Ser878insGluSer
XR_945604.3:n.2873_2874insGGAGTC
XR_945605.3:n.2873_2874insGGAGTC