Canonical Allele Identifier: CA449667202

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625845C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658068C>T , CM000668.2:g.31658068C>T	GRCh38
NC_000006.11:g.31625845C>T , CM000668.1:g.31625845C>T	GRCh37
NC_000006.10:g.31733824C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.546C>T (APOM) MANE Select	ENSP00000365081.3:p.Ala182=
ENST00000375916.3:c.546C>T (APOM)	ENSP00000365081.3:p.Ala182=
ENST00000375918.6:c.*280C>T (APOM)	ENSP00000365083.2:n.*280C>T
ENST00000375920.8:c.330C>T (APOM)	ENSP00000365085.4:p.Ala110=
NM_001256169.1:c.330C>T (APOM)	NP_001243098.1:p.Ala110=
NM_019101.2:c.546C>T (APOM)	NP_061974.2:p.Ala182=
NR_045828.1:n.581C>T (APOM)
XM_006715150.2:c.450C>T (APOM)	XP_006715213.1:p.Ala150=
XM_011514895.1:c.-14+2253G>A (BAG6)	XP_011513197.1:n.-14+2253G>A
XM_006715150.3:c.450C>T (APOM)	XP_006715213.1:p.Ala150=
XM_017011279.2:c.-14+2253G>A (BAG6)	XP_016866768.1:n.-14+2253G>A
NM_019101.3:c.546C>T (APOM) MANE Select	NP_061974.2:p.Ala182=
NM_001256169.2:c.330C>T (APOM)	NP_001243098.1:p.Ala110=
NR_045828.2:n.587C>T (APOM)