Canonical Allele Identifier: CA363431581

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625844C>G (hg19) ; chr6:g.31658067C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658067C>G , CM000668.2:g.31658067C>G	GRCh38
NC_000006.11:g.31625844C>G , CM000668.1:g.31625844C>G	GRCh37
NC_000006.10:g.31733823C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.545C>G (APOM) MANE Select	ENSP00000365081.3:p.Ala182Gly
ENST00000375916.3:c.545C>G (APOM)	ENSP00000365081.3:p.Ala182Gly
ENST00000375918.6:c.*279C>G (APOM)	ENSP00000365083.2:n.*279C>G
ENST00000375920.8:c.329C>G (APOM)	ENSP00000365085.4:p.Ala110Gly
NM_001256169.1:c.329C>G (APOM)	NP_001243098.1:p.Ala110Gly
NM_019101.2:c.545C>G (APOM)	NP_061974.2:p.Ala182Gly
NR_045828.1:n.580C>G (APOM)
XM_006715150.2:c.449C>G (APOM)	XP_006715213.1:p.Ala150Gly
XM_011514895.1:c.-14+2254G>C (BAG6)	XP_011513197.1:n.-14+2254G>C
XM_006715150.3:c.449C>G (APOM)	XP_006715213.1:p.Ala150Gly
XM_017011279.2:c.-14+2254G>C (BAG6)	XP_016866768.1:n.-14+2254G>C
NM_019101.3:c.545C>G (APOM) MANE Select	NP_061974.2:p.Ala182Gly
NM_001256169.2:c.329C>G (APOM)	NP_001243098.1:p.Ala110Gly
NR_045828.2:n.586C>G (APOM)