Canonical Allele Identifier: CA2789199818

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845915_99845916insGGA , CM000672.2:g.99845915_99845916insGGA	GRCh38
NC_000010.10:g.101605672_101605673insGGA , CM000672.1:g.101605672_101605673insGGA	GRCh37
NC_000010.9:g.101595662_101595663insGGA	NCBI36
NG_011798.1:g.68210_68211insGGA
NG_011798.2:g.68318_68319insGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+133_4146+134insGGA MANE Select	ENSP00000497274.1:n.4146+133_4146+134insGGA
ENST00000648523.1:c.34+133_34+134insGGA
ENST00000649459.1:n.494+133_494+134insGGA
ENST00000370449.8:c.4146+133_4146+134insGGA	ENSP00000359478.4:n.4146+133_4146+134insGGA
NM_000392.4:c.4146+133_4146+134insGGA	NP_000383.1:n.4146+133_4146+134insGGA
XM_006717630.2:c.3450+133_3450+134insGGA	XP_006717693.1:n.3450+133_3450+134insGGA
XR_945604.1:n.4276+133_4276+134insGGA
XR_945605.1:n.4210+133_4210+134insGGA
NM_000392.5:c.4146+133_4146+134insGGA MANE Select	NP_000383.2:n.4146+133_4146+134insGGA
XM_006717630.3:c.3450+133_3450+134insGGA	XP_006717693.1:n.3450+133_3450+134insGGA
XR_945604.3:n.4330+133_4330+134insGGA
XR_945605.3:n.4262+133_4262+134insGGA