Canonical Allele Identifier: CA449666899

Gene: APOM BAG6

Linked Data

• COSMIC: COSM6445053 ; COSM6445054
• MyVariant Identifiers: chr6:g.31625024C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657247C>A , CM000668.2:g.31657247C>A	GRCh38
NC_000006.11:g.31625024C>A , CM000668.1:g.31625024C>A	GRCh37
NC_000006.10:g.31733003C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.292C>A (APOM) MANE Select	ENSP00000365081.3:p.Arg98=
ENST00000375916.3:c.292C>A (APOM)	ENSP00000365081.3:p.Arg98=
ENST00000375918.6:c.76C>A (APOM)	ENSP00000365083.2:p.Arg26=
ENST00000375920.8:c.76C>A (APOM)	ENSP00000365085.4:p.Arg26=
NM_001256169.1:c.76C>A (APOM)	NP_001243098.1:p.Arg26=
NM_019101.2:c.292C>A (APOM)	NP_061974.2:p.Arg98=
NR_045828.1:n.327C>A (APOM)
XM_006715150.2:c.196C>A (APOM)	XP_006715213.1:p.Arg66=
XM_011514895.1:c.-14+3074G>T (BAG6)	XP_011513197.1:n.-14+3074G>T
XM_006715150.3:c.196C>A (APOM)	XP_006715213.1:p.Arg66=
XM_017011279.2:c.-14+3074G>T (BAG6)	XP_016866768.1:n.-14+3074G>T
XM_024446545.1:c.-14+517G>T (BAG6)	XP_024302313.1:n.-14+517G>T
NM_019101.3:c.292C>A (APOM) MANE Select	NP_061974.2:p.Arg98=
NM_001256169.2:c.76C>A (APOM)	NP_001243098.1:p.Arg26=
NR_045828.2:n.333C>A (APOM)