Canonical Allele Identifier: CA363430079

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625410C>A (hg19) ; chr6:g.31657633C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657633C>A , CM000668.2:g.31657633C>A	GRCh38
NC_000006.11:g.31625410C>A , CM000668.1:g.31625410C>A	GRCh37
NC_000006.10:g.31733389C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.451C>A (APOM) MANE Select	ENSP00000365081.3:p.Pro151Thr
ENST00000375916.3:c.451C>A (APOM)	ENSP00000365081.3:p.Pro151Thr
ENST00000375918.6:c.235C>A (APOM)	ENSP00000365083.2:p.Pro79Thr
ENST00000375920.8:c.235C>A (APOM)	ENSP00000365085.4:p.Pro79Thr
NM_001256169.1:c.235C>A (APOM)	NP_001243098.1:p.Pro79Thr
NM_019101.2:c.451C>A (APOM)	NP_061974.2:p.Pro151Thr
NR_045828.1:n.486C>A (APOM)
XM_006715150.2:c.355C>A (APOM)	XP_006715213.1:p.Pro119Thr
XM_011514895.1:c.-14+2688G>T (BAG6)	XP_011513197.1:n.-14+2688G>T
XM_006715150.3:c.355C>A (APOM)	XP_006715213.1:p.Pro119Thr
XM_017011279.2:c.-14+2688G>T (BAG6)	XP_016866768.1:n.-14+2688G>T
XM_024446545.1:c.-14+131G>T (BAG6)	XP_024302313.1:n.-14+131G>T
NM_019101.3:c.451C>A (APOM) MANE Select	NP_061974.2:p.Pro151Thr
NM_001256169.2:c.235C>A (APOM)	NP_001243098.1:p.Pro79Thr
NR_045828.2:n.492C>A (APOM)