Canonical Allele Identifier: CA1931495991

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836047_99836048delinsCT , CM000672.2:g.99836047_99836048delinsCT	GRCh38
NC_000010.10:g.101595804_101595805delinsCT , CM000672.1:g.101595804_101595805delinsCT	GRCh37
NC_000010.9:g.101585794_101585795delinsCT	NCBI36
NG_011798.1:g.58342_58343delinsCT
NG_011798.2:g.58450_58451delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3415-44_3415-43delinsCT MANE Select	ENSP00000497274.1:n.3415-44_3415-43delinsCT
ENST00000370449.8:c.3415-44_3415-43delinsCT	ENSP00000359478.4:n.3415-44_3415-43delinsCT
NM_000392.4:c.3415-44_3415-43delinsCT	NP_000383.1:n.3415-44_3415-43delinsCT
XM_006717630.2:c.2719-44_2719-43delinsCT	XP_006717693.1:n.2719-44_2719-43delinsCT
XR_945604.1:n.3604-44_3604-43delinsCT
XR_945605.1:n.3606-44_3606-43delinsCT
NM_000392.5:c.3415-44_3415-43delinsCT MANE Select	NP_000383.2:n.3415-44_3415-43delinsCT
XM_006717630.3:c.2719-44_2719-43delinsCT	XP_006717693.1:n.2719-44_2719-43delinsCT
XR_945604.3:n.3658-44_3658-43delinsCT
XR_945605.3:n.3658-44_3658-43delinsCT