Canonical Allele Identifier: CA2523834465

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830276_99830277insG , CM000672.2:g.99830276_99830277insG	GRCh38
NC_000010.10:g.101590033_101590034insG , CM000672.1:g.101590033_101590034insG	GRCh37
NC_000010.9:g.101580023_101580024insG	NCBI36
NG_011798.1:g.52571_52572insG
NG_011798.2:g.52679_52680insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2621-31_2621-30insG MANE Select	ENSP00000497274.1:n.2621-31_2621-30insG
ENST00000370449.8:c.2621-31_2621-30insG	ENSP00000359478.4:n.2621-31_2621-30insG
NM_000392.4:c.2621-31_2621-30insG	NP_000383.1:n.2621-31_2621-30insG
XM_006717630.2:c.1925-31_1925-30insG	XP_006717693.1:n.1925-31_1925-30insG
XM_006717631.2:c.*48-31_*48-30insG	XP_006717694.1:n.*48-31_*48-30insG
XM_011539291.1:c.2621-31_2621-30insG	XP_011537593.1:n.2621-31_2621-30insG
XR_945604.1:n.2810-31_2810-30insG
XR_945605.1:n.2812-31_2812-30insG
NM_000392.5:c.2621-31_2621-30insG MANE Select	NP_000383.2:n.2621-31_2621-30insG
XM_006717630.3:c.1925-31_1925-30insG	XP_006717693.1:n.1925-31_1925-30insG
XM_006717631.4:c.*48-31_*48-30insG	XP_006717694.1:n.*48-31_*48-30insG
XM_011539291.3:c.2621-31_2621-30insG	XP_011537593.1:n.2621-31_2621-30insG
XR_945604.3:n.2864-31_2864-30insG
XR_945605.3:n.2864-31_2864-30insG