Canonical Allele Identifier: CA449667150

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657704-A-G
• MyVariant Identifiers: chr6:g.31625481A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657704A>G , CM000668.2:g.31657704A>G	GRCh38
NC_000006.11:g.31625481A>G , CM000668.1:g.31625481A>G	GRCh37
NC_000006.10:g.31733460A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.522A>G (APOM) MANE Select	ENSP00000365081.3:p.Leu174=
ENST00000375916.3:c.522A>G (APOM)	ENSP00000365081.3:p.Leu174=
ENST00000375918.6:c.306A>G (APOM)	ENSP00000365083.2:p.Leu102=
ENST00000375920.8:c.306A>G (APOM)	ENSP00000365085.4:p.Leu102=
NM_001256169.1:c.306A>G (APOM)	NP_001243098.1:p.Leu102=
NM_019101.2:c.522A>G (APOM)	NP_061974.2:p.Leu174=
NR_045828.1:n.557A>G (APOM)
XM_006715150.2:c.426A>G (APOM)	XP_006715213.1:p.Leu142=
XM_011514895.1:c.-14+2617T>C (BAG6)	XP_011513197.1:n.-14+2617T>C
XM_006715150.3:c.426A>G (APOM)	XP_006715213.1:p.Leu142=
XM_017011279.2:c.-14+2617T>C (BAG6)	XP_016866768.1:n.-14+2617T>C
XM_024446545.1:c.-14+60T>C (BAG6)	XP_024302313.1:n.-14+60T>C
NM_019101.3:c.522A>G (APOM) MANE Select	NP_061974.2:p.Leu174=
NM_001256169.2:c.306A>G (APOM)	NP_001243098.1:p.Leu102=
NR_045828.2:n.563A>G (APOM)