Canonical Allele Identifier: CA1619251003

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658157_31658158delinsGA , CM000668.2:g.31658157_31658158delinsGA	GRCh38
NC_000006.11:g.31625934_31625935delinsGA , CM000668.1:g.31625934_31625935delinsGA	GRCh37
NC_000006.10:g.31733913_31733914delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*68_*69delinsGA (APOM) MANE Select	ENSP00000365081.3:n.*68_*69delinsGA
ENST00000375916.3:c.*68_*69delinsGA (APOM)	ENSP00000365081.3:n.*68_*69delinsGA
ENST00000375920.8:c.*68_*69delinsGA (APOM)	ENSP00000365085.4:n.*68_*69delinsGA
NM_001256169.1:c.*68_*69delinsGA (APOM)	NP_001243098.1:n.*68_*69delinsGA
NM_019101.2:c.*68_*69delinsGA (APOM)	NP_061974.2:n.*68_*69delinsGA
NR_045828.1:n.670_671delinsGA (APOM)
XM_006715150.2:c.*68_*69delinsGA (APOM)	XP_006715213.1:n.*68_*69delinsGA
XM_011514895.1:c.-14+2163_-14+2164delinsTC (BAG6)	XP_011513197.1:n.-14+2163_-14+2164delinsTC
XM_006715150.3:c.*68_*69delinsGA (APOM)	XP_006715213.1:n.*68_*69delinsGA
XM_017011279.2:c.-14+2163_-14+2164delinsTC (BAG6)	XP_016866768.1:n.-14+2163_-14+2164delinsTC
NM_019101.3:c.*68_*69delinsGA (APOM) MANE Select	NP_061974.2:n.*68_*69delinsGA
NM_001256169.2:c.*68_*69delinsGA (APOM)	NP_001243098.1:n.*68_*69delinsGA
NR_045828.2:n.676_677delinsGA (APOM)