Canonical Allele Identifier: CA2789199822

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845918_99845919insGGGATA , CM000672.2:g.99845918_99845919insGGGATA	GRCh38
NC_000010.10:g.101605675_101605676insGGGATA , CM000672.1:g.101605675_101605676insGGGATA	GRCh37
NC_000010.9:g.101595665_101595666insGGGATA	NCBI36
NG_011798.1:g.68213_68214insGGGATA
NG_011798.2:g.68321_68322insGGGATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+136_4146+137insGGGATA MANE Select	ENSP00000497274.1:n.4146+136_4146+137insGGGATA
ENST00000648523.1:c.34+136_34+137insGGGATA
ENST00000649459.1:n.494+136_494+137insGGGATA
ENST00000370449.8:c.4146+136_4146+137insGGGATA	ENSP00000359478.4:n.4146+136_4146+137insGGGATA
NM_000392.4:c.4146+136_4146+137insGGGATA	NP_000383.1:n.4146+136_4146+137insGGGATA
XM_006717630.2:c.3450+136_3450+137insGGGATA	XP_006717693.1:n.3450+136_3450+137insGGGATA
XR_945604.1:n.4276+136_4276+137insGGGATA
XR_945605.1:n.4210+136_4210+137insGGGATA
NM_000392.5:c.4146+136_4146+137insGGGATA MANE Select	NP_000383.2:n.4146+136_4146+137insGGGATA
XM_006717630.3:c.3450+136_3450+137insGGGATA	XP_006717693.1:n.3450+136_3450+137insGGGATA
XR_945604.3:n.4330+136_4330+137insGGGATA
XR_945605.3:n.4262+136_4262+137insGGGATA