Canonical Allele Identifier: CA2610497933

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845849-GCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845856_99845858del , CM000672.2:g.99845856_99845858del	GRCh38
NC_000010.10:g.101605613_101605615del , CM000672.1:g.101605613_101605615del	GRCh37
NC_000010.9:g.101595603_101595605del	NCBI36
NG_011798.1:g.68151_68153del
NG_011798.2:g.68259_68261del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+74_4146+76del MANE Select	ENSP00000497274.1:n.4146+74_4146+76del
ENST00000648523.1:c.34+74_34+76del
ENST00000649459.1:n.494+74_494+76del
ENST00000370449.8:c.4146+74_4146+76del	ENSP00000359478.4:n.4146+74_4146+76del
NM_000392.4:c.4146+74_4146+76del	NP_000383.1:n.4146+74_4146+76del
XM_006717630.2:c.3450+74_3450+76del	XP_006717693.1:n.3450+74_3450+76del
XR_945604.1:n.4276+74_4276+76del
XR_945605.1:n.4210+74_4210+76del
NM_000392.5:c.4146+74_4146+76del MANE Select	NP_000383.2:n.4146+74_4146+76del
XM_006717630.3:c.3450+74_3450+76del	XP_006717693.1:n.3450+74_3450+76del
XR_945604.3:n.4330+74_4330+76del
XR_945605.3:n.4262+74_4262+76del