Canonical Allele Identifier: CA2677983897

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657632-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657634dup , CM000668.2:g.31657634dup	GRCh38
NC_000006.11:g.31625411dup , CM000668.1:g.31625411dup	GRCh37
NC_000006.10:g.31733390dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.452dup (APOM) MANE Select	ENSP00000365081.3:p.His152ThrfsTer27
ENST00000375916.3:c.452dup (APOM)	ENSP00000365081.3:p.His152ThrfsTer27
ENST00000375918.6:c.236dup (APOM)	ENSP00000365083.2:p.His80ThrfsTer27
ENST00000375920.8:c.236dup (APOM)	ENSP00000365085.4:p.His80ThrfsTer27
NM_001256169.1:c.236dup (APOM)	NP_001243098.1:p.His80ThrfsTer27
NM_019101.2:c.452dup (APOM)	NP_061974.2:p.His152ThrfsTer27
NR_045828.1:n.487dup (APOM)
XM_006715150.2:c.356dup (APOM)	XP_006715213.1:p.His120ThrfsTer27
XM_011514895.1:c.-14+2688dup (BAG6)	XP_011513197.1:n.-14+2688dup
XM_006715150.3:c.356dup (APOM)	XP_006715213.1:p.His120ThrfsTer27
XM_017011279.2:c.-14+2688dup (BAG6)	XP_016866768.1:n.-14+2688dup
XM_024446545.1:c.-14+131dup (BAG6)	XP_024302313.1:n.-14+131dup
NM_019101.3:c.452dup (APOM) MANE Select	NP_061974.2:p.His152ThrfsTer27
NM_001256169.2:c.236dup (APOM)	NP_001243098.1:p.His80ThrfsTer27
NR_045828.2:n.493dup (APOM)