Canonical Allele Identifier: CA449667110

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625421C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657644C>A , CM000668.2:g.31657644C>A	GRCh38
NC_000006.11:g.31625421C>A , CM000668.1:g.31625421C>A	GRCh37
NC_000006.10:g.31733400C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.462C>A (APOM) MANE Select	ENSP00000365081.3:p.Pro154=
ENST00000375916.3:c.462C>A (APOM)	ENSP00000365081.3:p.Pro154=
ENST00000375918.6:c.246C>A (APOM)	ENSP00000365083.2:p.Pro82=
ENST00000375920.8:c.246C>A (APOM)	ENSP00000365085.4:p.Pro82=
NM_001256169.1:c.246C>A (APOM)	NP_001243098.1:p.Pro82=
NM_019101.2:c.462C>A (APOM)	NP_061974.2:p.Pro154=
NR_045828.1:n.497C>A (APOM)
XM_006715150.2:c.366C>A (APOM)	XP_006715213.1:p.Pro122=
XM_011514895.1:c.-14+2677G>T (BAG6)	XP_011513197.1:n.-14+2677G>T
XM_006715150.3:c.366C>A (APOM)	XP_006715213.1:p.Pro122=
XM_017011279.2:c.-14+2677G>T (BAG6)	XP_016866768.1:n.-14+2677G>T
XM_024446545.1:c.-14+120G>T (BAG6)	XP_024302313.1:n.-14+120G>T
NM_019101.3:c.462C>A (APOM) MANE Select	NP_061974.2:p.Pro154=
NM_001256169.2:c.246C>A (APOM)	NP_001243098.1:p.Pro82=
NR_045828.2:n.503C>A (APOM)