Canonical Allele Identifier: CA363430539

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625453C>A (hg19) ; chr6:g.31657676C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657676C>A , CM000668.2:g.31657676C>A	GRCh38
NC_000006.11:g.31625453C>A , CM000668.1:g.31625453C>A	GRCh37
NC_000006.10:g.31733432C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.494C>A (APOM) MANE Select	ENSP00000365081.3:p.Thr165Asn
ENST00000375916.3:c.494C>A (APOM)	ENSP00000365081.3:p.Thr165Asn
ENST00000375918.6:c.278C>A (APOM)	ENSP00000365083.2:p.Thr93Asn
ENST00000375920.8:c.278C>A (APOM)	ENSP00000365085.4:p.Thr93Asn
NM_001256169.1:c.278C>A (APOM)	NP_001243098.1:p.Thr93Asn
NM_019101.2:c.494C>A (APOM)	NP_061974.2:p.Thr165Asn
NR_045828.1:n.529C>A (APOM)
XM_006715150.2:c.398C>A (APOM)	XP_006715213.1:p.Thr133Asn
XM_011514895.1:c.-14+2645G>T (BAG6)	XP_011513197.1:n.-14+2645G>T
XM_006715150.3:c.398C>A (APOM)	XP_006715213.1:p.Thr133Asn
XM_017011279.2:c.-14+2645G>T (BAG6)	XP_016866768.1:n.-14+2645G>T
XM_024446545.1:c.-14+88G>T (BAG6)	XP_024302313.1:n.-14+88G>T
NM_019101.3:c.494C>A (APOM) MANE Select	NP_061974.2:p.Thr165Asn
NM_001256169.2:c.278C>A (APOM)	NP_001243098.1:p.Thr93Asn
NR_045828.2:n.535C>A (APOM)