Canonical Allele Identifier: CA2574638622
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836387del , CM000672.2:g.99836387del GRCh38
NC_000010.10:g.101596144del , CM000672.1:g.101596144del GRCh37
NC_000010.9:g.101586134del NCBI36
NG_011798.1:g.58682del
NG_011798.2:g.58790del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3614+97del MANE Select ENSP00000497274.1:n.3614+97del
ENST00000370449.8:c.3614+97del ENSP00000359478.4:n.3614+97del
NM_000392.4:c.3614+97del NP_000383.1:n.3614+97del
XM_006717630.2:c.2918+97del XP_006717693.1:n.2918+97del
XR_945604.1:n.3803+97del
XR_945605.1:n.3805+97del
NM_000392.5:c.3614+97del MANE Select NP_000383.2:n.3614+97del
XM_006717630.3:c.2918+97del XP_006717693.1:n.2918+97del
XR_945604.3:n.3857+97del
XR_945605.3:n.3857+97del