Canonical Allele Identifier: CA1931513906
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845681_99845699delinsAGAATCTTAGAGGCTGCCG , CM000672.2:g.99845681_99845699delinsAGAATCTTAGAGGCTGCCG GRCh38
NC_000010.10:g.101605438_101605456delinsAGAATCTTAGAGGCTGCCG , CM000672.1:g.101605438_101605456delinsAGAATCTTAGAGGCTGCCG GRCh37
NC_000010.9:g.101595428_101595446delinsAGAATCTTAGAGGCTGCCG NCBI36
NG_011798.1:g.67976_67994delinsAGAATCTTAGAGGCTGCCG
NG_011798.2:g.68084_68102delinsAGAATCTTAGAGGCTGCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4045_4063delinsAGAATCTTAGAGGCTGCCG MANE Select ENSP00000497274.1:p.Arg1349=
ENST00000649459.1:n.393_411delinsAGAATCTTAGAGGCTGCCG
ENST00000370449.8:c.4045_4063delinsAGAATCTTAGAGGCTGCCG ENSP00000359478.4:p.Arg1349=
NM_000392.4:c.4045_4063delinsAGAATCTTAGAGGCTGCCG NP_000383.1:p.Arg1349=
XM_006717630.2:c.3349_3367delinsAGAATCTTAGAGGCTGCCG XP_006717693.1:p.Arg1117=
XR_945604.1:n.4177-2_4193delinsAGAATCTTAGAGGCTGCCG
XR_945605.1:n.4109_4127delinsAGAATCTTAGAGGCTGCCG
NM_000392.5:c.4045_4063delinsAGAATCTTAGAGGCTGCCG MANE Select NP_000383.2:p.Arg1349=
XM_006717630.3:c.3349_3367delinsAGAATCTTAGAGGCTGCCG XP_006717693.1:p.Arg1117=
XR_945604.3:n.4231-2_4247delinsAGAATCTTAGAGGCTGCCG
XR_945605.3:n.4161_4179delinsAGAATCTTAGAGGCTGCCG