Canonical Allele Identifier: CA2522607171
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830267del , CM000672.2:g.99830267del GRCh38
NC_000010.10:g.101590024del , CM000672.1:g.101590024del GRCh37
NC_000010.9:g.101580014del NCBI36
NG_011798.1:g.52562del
NG_011798.2:g.52670del

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.2621-40del MANE Select ENSP00000497274.1:n.2621-40del
ENST00000370449.8:c.2621-40del ENSP00000359478.4:n.2621-40del
NM_000392.4:c.2621-40del NP_000383.1:n.2621-40del
XM_006717630.2:c.1925-40del XP_006717693.1:n.1925-40del
XM_006717631.2:c.*48-40del XP_006717694.1:n.*48-40del
XM_011539291.1:c.2621-40del XP_011537593.1:n.2621-40del
XR_945604.1:n.2810-40del
XR_945605.1:n.2812-40del
NM_000392.5:c.2621-40del MANE Select NP_000383.2:n.2621-40del
XM_006717630.3:c.1925-40del XP_006717693.1:n.1925-40del
XM_006717631.4:c.*48-40del XP_006717694.1:n.*48-40del
XM_011539291.3:c.2621-40del XP_011537593.1:n.2621-40del
XR_945604.3:n.2864-40del
XR_945605.3:n.2864-40del