Canonical Allele Identifier: CA363426938

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625022C>G (hg19) ; chr6:g.31657245C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657245C>G , CM000668.2:g.31657245C>G	GRCh38
NC_000006.11:g.31625022C>G , CM000668.1:g.31625022C>G	GRCh37
NC_000006.10:g.31733001C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.290C>G (APOM) MANE Select	ENSP00000365081.3:p.Pro97Arg
ENST00000375916.3:c.290C>G (APOM)	ENSP00000365081.3:p.Pro97Arg
ENST00000375918.6:c.74C>G (APOM)	ENSP00000365083.2:p.Pro25Arg
ENST00000375920.8:c.74C>G (APOM)	ENSP00000365085.4:p.Pro25Arg
NM_001256169.1:c.74C>G (APOM)	NP_001243098.1:p.Pro25Arg
NM_019101.2:c.290C>G (APOM)	NP_061974.2:p.Pro97Arg
NR_045828.1:n.325C>G (APOM)
XM_006715150.2:c.194C>G (APOM)	XP_006715213.1:p.Pro65Arg
XM_011514895.1:c.-14+3076G>C (BAG6)	XP_011513197.1:n.-14+3076G>C
XM_006715150.3:c.194C>G (APOM)	XP_006715213.1:p.Pro65Arg
XM_017011279.2:c.-14+3076G>C (BAG6)	XP_016866768.1:n.-14+3076G>C
XM_024446545.1:c.-14+519G>C (BAG6)	XP_024302313.1:n.-14+519G>C
NM_019101.3:c.290C>G (APOM) MANE Select	NP_061974.2:p.Pro97Arg
NM_001256169.2:c.74C>G (APOM)	NP_001243098.1:p.Pro25Arg
NR_045828.2:n.331C>G (APOM)