Canonical Allele Identifier: CA2574638607
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836333del , CM000672.2:g.99836333del GRCh38
NC_000010.10:g.101596090del , CM000672.1:g.101596090del GRCh37
NC_000010.9:g.101586080del NCBI36
NG_011798.1:g.58628del
NG_011798.2:g.58736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3614+43del MANE Select ENSP00000497274.1:n.3614+43del
ENST00000370449.8:c.3614+43del ENSP00000359478.4:n.3614+43del
NM_000392.4:c.3614+43del NP_000383.1:n.3614+43del
XM_006717630.2:c.2918+43del XP_006717693.1:n.2918+43del
XR_945604.1:n.3803+43del
XR_945605.1:n.3805+43del
NM_000392.5:c.3614+43del MANE Select NP_000383.2:n.3614+43del
XM_006717630.3:c.2918+43del XP_006717693.1:n.2918+43del
XR_945604.3:n.3857+43del
XR_945605.3:n.3857+43del