Canonical Allele Identifier: CA1931496016

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836072_99836073delinsCT , CM000672.2:g.99836072_99836073delinsCT	GRCh38
NC_000010.10:g.101595829_101595830delinsCT , CM000672.1:g.101595829_101595830delinsCT	GRCh37
NC_000010.9:g.101585819_101585820delinsCT	NCBI36
NG_011798.1:g.58367_58368delinsCT
NG_011798.2:g.58475_58476delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-19_3415-18delinsCT MANE Select	ENSP00000497274.1:n.3415-19_3415-18delinsCT
ENST00000370449.8:c.3415-19_3415-18delinsCT	ENSP00000359478.4:n.3415-19_3415-18delinsCT
NM_000392.4:c.3415-19_3415-18delinsCT	NP_000383.1:n.3415-19_3415-18delinsCT
XM_006717630.2:c.2719-19_2719-18delinsCT	XP_006717693.1:n.2719-19_2719-18delinsCT
XR_945604.1:n.3604-19_3604-18delinsCT
XR_945605.1:n.3606-19_3606-18delinsCT
NM_000392.5:c.3415-19_3415-18delinsCT MANE Select	NP_000383.2:n.3415-19_3415-18delinsCT
XM_006717630.3:c.2719-19_2719-18delinsCT	XP_006717693.1:n.2719-19_2719-18delinsCT
XR_945604.3:n.3658-19_3658-18delinsCT
XR_945605.3:n.3658-19_3658-18delinsCT