Canonical Allele Identifier: CA363430426

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625441T>A (hg19) ; chr6:g.31657664T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657664T>A , CM000668.2:g.31657664T>A	GRCh38
NC_000006.11:g.31625441T>A , CM000668.1:g.31625441T>A	GRCh37
NC_000006.10:g.31733420T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.482T>A (APOM) MANE Select	ENSP00000365081.3:p.Phe161Tyr
ENST00000375916.3:c.482T>A (APOM)	ENSP00000365081.3:p.Phe161Tyr
ENST00000375918.6:c.266T>A (APOM)	ENSP00000365083.2:p.Phe89Tyr
ENST00000375920.8:c.266T>A (APOM)	ENSP00000365085.4:p.Phe89Tyr
NM_001256169.1:c.266T>A (APOM)	NP_001243098.1:p.Phe89Tyr
NM_019101.2:c.482T>A (APOM)	NP_061974.2:p.Phe161Tyr
NR_045828.1:n.517T>A (APOM)
XM_006715150.2:c.386T>A (APOM)	XP_006715213.1:p.Phe129Tyr
XM_011514895.1:c.-14+2657A>T (BAG6)	XP_011513197.1:n.-14+2657A>T
XM_006715150.3:c.386T>A (APOM)	XP_006715213.1:p.Phe129Tyr
XM_017011279.2:c.-14+2657A>T (BAG6)	XP_016866768.1:n.-14+2657A>T
XM_024446545.1:c.-14+100A>T (BAG6)	XP_024302313.1:n.-14+100A>T
NM_019101.3:c.482T>A (APOM) MANE Select	NP_061974.2:p.Phe161Tyr
NM_001256169.2:c.266T>A (APOM)	NP_001243098.1:p.Phe89Tyr
NR_045828.2:n.523T>A (APOM)