Canonical Allele Identifier: CA1931495667

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835722_99835723delinsAT , CM000672.2:g.99835722_99835723delinsAT	GRCh38
NC_000010.10:g.101595479_101595480delinsAT , CM000672.1:g.101595479_101595480delinsAT	GRCh37
NC_000010.9:g.101585469_101585470delinsAT	NCBI36
NG_011798.1:g.58017_58018delinsAT
NG_011798.2:g.58125_58126delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-369_3415-368delinsAT MANE Select	ENSP00000497274.1:n.3415-369_3415-368delinsAT
ENST00000370449.8:c.3415-369_3415-368delinsAT	ENSP00000359478.4:n.3415-369_3415-368delinsAT
NM_000392.4:c.3415-369_3415-368delinsAT	NP_000383.1:n.3415-369_3415-368delinsAT
XM_006717630.2:c.2719-369_2719-368delinsAT	XP_006717693.1:n.2719-369_2719-368delinsAT
XR_945604.1:n.3604-369_3604-368delinsAT
XR_945605.1:n.3606-369_3606-368delinsAT
NM_000392.5:c.3415-369_3415-368delinsAT MANE Select	NP_000383.2:n.3415-369_3415-368delinsAT
XM_006717630.3:c.2719-369_2719-368delinsAT	XP_006717693.1:n.2719-369_2719-368delinsAT
XR_945604.3:n.3658-369_3658-368delinsAT
XR_945605.3:n.3658-369_3658-368delinsAT