Canonical Allele Identifier: CA2677982458

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31655887-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655887_31655888insC , CM000668.2:g.31655887_31655888insC	GRCh38
NC_000006.11:g.31623664_31623665insC , CM000668.1:g.31623664_31623665insC	GRCh37
NC_000006.10:g.31731643_31731644insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-80_-79insC (APOM)	ENSP00000365081.3:n.-80_-79insC
ENST00000375918.6:c.-102-585_-102-584insC (APOM)	ENSP00000365083.2:n.-102-585_-102-584insC
ENST00000375920.8:c.-102-585_-102-584insC (APOM)	ENSP00000365085.4:n.-102-585_-102-584insC
NM_001256169.1:c.-102-585_-102-584insC (APOM)	NP_001243098.1:n.-102-585_-102-584insC
NR_045828.1:n.143-585_143-584insC (APOM)
XM_006715150.2:c.-183_-182insC (APOM)	XP_006715213.1:n.-183_-182insC
XM_011514895.1:c.-13-4112_-13-4111insG (BAG6)	XP_011513197.1:n.-13-4112_-13-4111insG
XM_017011279.2:c.-13-4112_-13-4111insG (BAG6)	XP_016866768.1:n.-13-4112_-13-4111insG
XM_024446545.1:c.-14+1876_-14+1877insG (BAG6)	XP_024302313.1:n.-14+1876_-14+1877insG
NM_001256169.2:c.-102-585_-102-584insC (APOM)	NP_001243098.1:n.-102-585_-102-584insC
NR_045828.2:n.149-585_149-584insC (APOM)