Canonical Allele Identifier: CA1931496013
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99836069_99836072delinsATTC , CM000672.2:g.99836069_99836072delinsATTC GRCh38
NC_000010.10:g.101595826_101595829delinsATTC , CM000672.1:g.101595826_101595829delinsATTC GRCh37
NC_000010.9:g.101585816_101585819delinsATTC NCBI36
NG_011798.1:g.58364_58367delinsATTC
NG_011798.2:g.58472_58475delinsATTC

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3415-22_3415-19delinsATTC MANE Select ENSP00000497274.1:n.3415-22_3415-19delinsATTC
ENST00000370449.8:c.3415-22_3415-19delinsATTC ENSP00000359478.4:n.3415-22_3415-19delinsATTC
NM_000392.4:c.3415-22_3415-19delinsATTC NP_000383.1:n.3415-22_3415-19delinsATTC
XM_006717630.2:c.2719-22_2719-19delinsATTC XP_006717693.1:n.2719-22_2719-19delinsATTC
XR_945604.1:n.3604-22_3604-19delinsATTC
XR_945605.1:n.3606-22_3606-19delinsATTC
NM_000392.5:c.3415-22_3415-19delinsATTC MANE Select NP_000383.2:n.3415-22_3415-19delinsATTC
XM_006717630.3:c.2719-22_2719-19delinsATTC XP_006717693.1:n.2719-22_2719-19delinsATTC
XR_945604.3:n.3658-22_3658-19delinsATTC
XR_945605.3:n.3658-22_3658-19delinsATTC