Canonical Allele Identifier: CA363430599

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625461C>A (hg19) ; chr6:g.31657684C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657684C>A , CM000668.2:g.31657684C>A	GRCh38
NC_000006.11:g.31625461C>A , CM000668.1:g.31625461C>A	GRCh37
NC_000006.10:g.31733440C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.502C>A (APOM) MANE Select	ENSP00000365081.3:p.Leu168Met
ENST00000375916.3:c.502C>A (APOM)	ENSP00000365081.3:p.Leu168Met
ENST00000375918.6:c.286C>A (APOM)	ENSP00000365083.2:p.Leu96Met
ENST00000375920.8:c.286C>A (APOM)	ENSP00000365085.4:p.Leu96Met
NM_001256169.1:c.286C>A (APOM)	NP_001243098.1:p.Leu96Met
NM_019101.2:c.502C>A (APOM)	NP_061974.2:p.Leu168Met
NR_045828.1:n.537C>A (APOM)
XM_006715150.2:c.406C>A (APOM)	XP_006715213.1:p.Leu136Met
XM_011514895.1:c.-14+2637G>T (BAG6)	XP_011513197.1:n.-14+2637G>T
XM_006715150.3:c.406C>A (APOM)	XP_006715213.1:p.Leu136Met
XM_017011279.2:c.-14+2637G>T (BAG6)	XP_016866768.1:n.-14+2637G>T
XM_024446545.1:c.-14+80G>T (BAG6)	XP_024302313.1:n.-14+80G>T
NM_019101.3:c.502C>A (APOM) MANE Select	NP_061974.2:p.Leu168Met
NM_001256169.2:c.286C>A (APOM)	NP_001243098.1:p.Leu96Met
NR_045828.2:n.543C>A (APOM)