Canonical Allele Identifier: CA2578566731

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656693_31656695dup , CM000668.2:g.31656693_31656695dup	GRCh38
NC_000006.11:g.31624470_31624472dup , CM000668.1:g.31624470_31624472dup	GRCh37
NC_000006.10:g.31732449_31732451dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.269+67_269+69dup (APOM) MANE Select	ENSP00000365081.3:n.269+67_269+69dup
ENST00000375916.3:c.269+67_269+69dup (APOM)	ENSP00000365081.3:n.269+67_269+69dup
ENST00000375918.6:c.53+67_53+69dup (APOM)	ENSP00000365083.2:n.53+67_53+69dup
ENST00000375920.8:c.53+67_53+69dup (APOM)	ENSP00000365085.4:n.53+67_53+69dup
NM_001256169.1:c.53+67_53+69dup (APOM)	NP_001243098.1:n.53+67_53+69dup
NM_019101.2:c.269+67_269+69dup (APOM)	NP_061974.2:n.269+67_269+69dup
NR_045828.1:n.304+60_304+62dup (APOM)
XM_006715150.2:c.173+60_173+62dup (APOM)	XP_006715213.1:n.173+60_173+62dup
XM_011514895.1:c.-14+3629_-14+3631dup (BAG6)	XP_011513197.1:n.-14+3629_-14+3631dup
XM_006715150.3:c.173+60_173+62dup (APOM)	XP_006715213.1:n.173+60_173+62dup
XM_017011279.2:c.-14+3629_-14+3631dup (BAG6)	XP_016866768.1:n.-14+3629_-14+3631dup
XM_024446545.1:c.-14+1072_-14+1074dup (BAG6)	XP_024302313.1:n.-14+1072_-14+1074dup
NM_019101.3:c.269+67_269+69dup (APOM) MANE Select	NP_061974.2:n.269+67_269+69dup
NM_001256169.2:c.53+67_53+69dup (APOM)	NP_001243098.1:n.53+67_53+69dup
NR_045828.2:n.310+60_310+62dup (APOM)