Canonical Allele Identifier: CA363426921

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625021C>A (hg19) ; chr6:g.31657244C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657244C>A , CM000668.2:g.31657244C>A	GRCh38
NC_000006.11:g.31625021C>A , CM000668.1:g.31625021C>A	GRCh37
NC_000006.10:g.31733000C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.289C>A (APOM) MANE Select	ENSP00000365081.3:p.Pro97Thr
ENST00000375916.3:c.289C>A (APOM)	ENSP00000365081.3:p.Pro97Thr
ENST00000375918.6:c.73C>A (APOM)	ENSP00000365083.2:p.Pro25Thr
ENST00000375920.8:c.73C>A (APOM)	ENSP00000365085.4:p.Pro25Thr
NM_001256169.1:c.73C>A (APOM)	NP_001243098.1:p.Pro25Thr
NM_019101.2:c.289C>A (APOM)	NP_061974.2:p.Pro97Thr
NR_045828.1:n.324C>A (APOM)
XM_006715150.2:c.193C>A (APOM)	XP_006715213.1:p.Pro65Thr
XM_011514895.1:c.-14+3077G>T (BAG6)	XP_011513197.1:n.-14+3077G>T
XM_006715150.3:c.193C>A (APOM)	XP_006715213.1:p.Pro65Thr
XM_017011279.2:c.-14+3077G>T (BAG6)	XP_016866768.1:n.-14+3077G>T
XM_024446545.1:c.-14+520G>T (BAG6)	XP_024302313.1:n.-14+520G>T
NM_019101.3:c.289C>A (APOM) MANE Select	NP_061974.2:p.Pro97Thr
NM_001256169.2:c.73C>A (APOM)	NP_001243098.1:p.Pro25Thr
NR_045828.2:n.330C>A (APOM)