Canonical Allele Identifier: CA1931495697
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99835738_99835743delinsTTTCTC , CM000672.2:g.99835738_99835743delinsTTTCTC GRCh38
NC_000010.10:g.101595495_101595500delinsTTTCTC , CM000672.1:g.101595495_101595500delinsTTTCTC GRCh37
NC_000010.9:g.101585485_101585490delinsTTTCTC NCBI36
NG_011798.1:g.58033_58038delinsTTTCTC
NG_011798.2:g.58141_58146delinsTTTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647814.1:c.3415-353_3415-348delinsTTTCTC MANE Select ENSP00000497274.1:n.3415-353_3415-348delinsTTTCTC
ENST00000370449.8:c.3415-353_3415-348delinsTTTCTC ENSP00000359478.4:n.3415-353_3415-348delinsTTTCTC
NM_000392.4:c.3415-353_3415-348delinsTTTCTC NP_000383.1:n.3415-353_3415-348delinsTTTCTC
XM_006717630.2:c.2719-353_2719-348delinsTTTCTC XP_006717693.1:n.2719-353_2719-348delinsTTTCTC
XR_945604.1:n.3604-353_3604-348delinsTTTCTC
XR_945605.1:n.3606-353_3606-348delinsTTTCTC
NM_000392.5:c.3415-353_3415-348delinsTTTCTC MANE Select NP_000383.2:n.3415-353_3415-348delinsTTTCTC
XM_006717630.3:c.2719-353_2719-348delinsTTTCTC XP_006717693.1:n.2719-353_2719-348delinsTTTCTC
XR_945604.3:n.3658-353_3658-348delinsTTTCTC
XR_945605.3:n.3658-353_3658-348delinsTTTCTC