Canonical Allele Identifier: CA2789198345
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99830516del , CM000672.2:g.99830516del GRCh38
NC_000010.10:g.101590273del , CM000672.1:g.101590273del GRCh37
NC_000010.9:g.101580263del NCBI36
NG_011798.1:g.52811del
NG_011798.2:g.52919del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.2747+83del MANE Select ENSP00000497274.1:n.2747+83del
ENST00000370449.8:c.2747+83del ENSP00000359478.4:n.2747+83del
NM_000392.4:c.2747+83del NP_000383.1:n.2747+83del
XM_006717630.2:c.2051+83del XP_006717693.1:n.2051+83del
XM_011539291.1:c.2747+83del XP_011537593.1:n.2747+83del
XR_945604.1:n.2936+83del
XR_945605.1:n.2938+83del
NM_000392.5:c.2747+83del MANE Select NP_000383.2:n.2747+83del
XM_006717630.3:c.2051+83del XP_006717693.1:n.2051+83del
XM_011539291.3:c.2747+83del XP_011537593.1:n.2747+83del
XR_945604.3:n.2990+83del
XR_945605.3:n.2990+83del