Canonical Allele Identifier: CA2838199299
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845672dup , CM000672.2:g.99845672dup GRCh38
NC_000010.10:g.101605429dup , CM000672.1:g.101605429dup GRCh37
NC_000010.9:g.101595419dup NCBI36
NG_011798.1:g.67967dup
NG_011798.2:g.68075dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.4036dup MANE Select ENSP00000497274.1:p.Cys1346LeufsTer16
ENST00000649459.1:n.384dup
ENST00000370449.8:c.4036dup ENSP00000359478.4:p.Cys1346LeufsTer16
NM_000392.4:c.4036dup NP_000383.1:p.Cys1346LeufsTer16
XM_006717630.2:c.3340dup XP_006717693.1:p.Cys1114LeufsTer16
XR_945604.1:n.4177-11dup
XR_945605.1:n.4100dup
NM_000392.5:c.4036dup MANE Select NP_000383.2:p.Cys1346LeufsTer16
XM_006717630.3:c.3340dup XP_006717693.1:p.Cys1114LeufsTer16
XR_945604.3:n.4231-11dup
XR_945605.3:n.4152dup