Canonical Allele Identifier: CA363430281

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625429G>T (hg19) ; chr6:g.31657652G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657652G>T , CM000668.2:g.31657652G>T	GRCh38
NC_000006.11:g.31625429G>T , CM000668.1:g.31625429G>T	GRCh37
NC_000006.10:g.31733408G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.470G>T (APOM) MANE Select	ENSP00000365081.3:p.Cys157Phe
ENST00000375916.3:c.470G>T (APOM)	ENSP00000365081.3:p.Cys157Phe
ENST00000375918.6:c.254G>T (APOM)	ENSP00000365083.2:p.Cys85Phe
ENST00000375920.8:c.254G>T (APOM)	ENSP00000365085.4:p.Cys85Phe
NM_001256169.1:c.254G>T (APOM)	NP_001243098.1:p.Cys85Phe
NM_019101.2:c.470G>T (APOM)	NP_061974.2:p.Cys157Phe
NR_045828.1:n.505G>T (APOM)
XM_006715150.2:c.374G>T (APOM)	XP_006715213.1:p.Cys125Phe
XM_011514895.1:c.-14+2669C>A (BAG6)	XP_011513197.1:n.-14+2669C>A
XM_006715150.3:c.374G>T (APOM)	XP_006715213.1:p.Cys125Phe
XM_017011279.2:c.-14+2669C>A (BAG6)	XP_016866768.1:n.-14+2669C>A
XM_024446545.1:c.-14+112C>A (BAG6)	XP_024302313.1:n.-14+112C>A
NM_019101.3:c.470G>T (APOM) MANE Select	NP_061974.2:p.Cys157Phe
NM_001256169.2:c.254G>T (APOM)	NP_001243098.1:p.Cys85Phe
NR_045828.2:n.511G>T (APOM)