Canonical Allele Identifier: CA363430618

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625464G>A (hg19) ; chr6:g.31657687G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657687G>A , CM000668.2:g.31657687G>A	GRCh38
NC_000006.11:g.31625464G>A , CM000668.1:g.31625464G>A	GRCh37
NC_000006.10:g.31733443G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.505G>A (APOM) MANE Select	ENSP00000365081.3:p.Asp169Asn
ENST00000375916.3:c.505G>A (APOM)	ENSP00000365081.3:p.Asp169Asn
ENST00000375918.6:c.289G>A (APOM)	ENSP00000365083.2:p.Asp97Asn
ENST00000375920.8:c.289G>A (APOM)	ENSP00000365085.4:p.Asp97Asn
NM_001256169.1:c.289G>A (APOM)	NP_001243098.1:p.Asp97Asn
NM_019101.2:c.505G>A (APOM)	NP_061974.2:p.Asp169Asn
NR_045828.1:n.540G>A (APOM)
XM_006715150.2:c.409G>A (APOM)	XP_006715213.1:p.Asp137Asn
XM_011514895.1:c.-14+2634C>T (BAG6)	XP_011513197.1:n.-14+2634C>T
XM_006715150.3:c.409G>A (APOM)	XP_006715213.1:p.Asp137Asn
XM_017011279.2:c.-14+2634C>T (BAG6)	XP_016866768.1:n.-14+2634C>T
XM_024446545.1:c.-14+77C>T (BAG6)	XP_024302313.1:n.-14+77C>T
NM_019101.3:c.505G>A (APOM) MANE Select	NP_061974.2:p.Asp169Asn
NM_001256169.2:c.289G>A (APOM)	NP_001243098.1:p.Asp97Asn
NR_045828.2:n.546G>A (APOM)