Canonical Allele Identifier: CA1619250001

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655697_31655698delinsTC , CM000668.2:g.31655697_31655698delinsTC	GRCh38
NC_000006.11:g.31623474_31623475delinsTC , CM000668.1:g.31623474_31623475delinsTC	GRCh37
NC_000006.10:g.31731453_31731454delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-270_-269delinsTC (APOM)	ENSP00000365081.3:n.-270_-269delinsTC
ENST00000375918.6:c.-102-775_-102-774delinsTC (APOM)	ENSP00000365083.2:n.-102-775_-102-774delinsTC
ENST00000375920.8:c.-102-775_-102-774delinsTC (APOM)	ENSP00000365085.4:n.-102-775_-102-774delinsTC
NM_001256169.1:c.-102-775_-102-774delinsTC (APOM)	NP_001243098.1:n.-102-775_-102-774delinsTC
NR_045828.1:n.143-775_143-774delinsTC (APOM)
XM_006715150.2:c.-373_-372delinsTC (APOM)	XP_006715213.1:n.-373_-372delinsTC
XM_011514895.1:c.-13-3922_-13-3921delinsGA (BAG6)	XP_011513197.1:n.-13-3922_-13-3921delinsGA
XM_017011279.2:c.-13-3922_-13-3921delinsGA (BAG6)	XP_016866768.1:n.-13-3922_-13-3921delinsGA
XM_024446545.1:c.-14+2066_-14+2067delinsGA (BAG6)	XP_024302313.1:n.-14+2066_-14+2067delinsGA
NM_001256169.2:c.-102-775_-102-774delinsTC (APOM)	NP_001243098.1:n.-102-775_-102-774delinsTC
NR_045828.2:n.149-775_149-774delinsTC (APOM)