Canonical Allele Identifier: CA1619250726

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657441T= , CM000668.2:g.31657441T=	GRCh38
NC_000006.11:g.31625218T= , CM000668.1:g.31625218T=	GRCh37
NC_000006.10:g.31733197T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.405T= (APOM) MANE Select	ENSP00000365081.3:p.Asn135=
ENST00000375916.3:c.405T= (APOM)	ENSP00000365081.3:p.Asn135=
ENST00000375918.6:c.189T= (APOM)	ENSP00000365083.2:p.Asn63=
ENST00000375920.8:c.189T= (APOM)	ENSP00000365085.4:p.Asn63=
NM_001256169.1:c.189T= (APOM)	NP_001243098.1:p.Asn63=
NM_019101.2:c.405T= (APOM)	NP_061974.2:p.Asn135=
NR_045828.1:n.440T= (APOM)
XM_006715150.2:c.309T= (APOM)	XP_006715213.1:p.Asn103=
XM_011514895.1:c.-14+2880A= (BAG6)	XP_011513197.1:n.-14+2880A=
XM_006715150.3:c.309T= (APOM)	XP_006715213.1:p.Asn103=
XM_017011279.2:c.-14+2880A= (BAG6)	XP_016866768.1:n.-14+2880A=
XM_024446545.1:c.-14+323A= (BAG6)	XP_024302313.1:n.-14+323A=
NM_019101.3:c.405T= (APOM) MANE Select	NP_061974.2:p.Asn135=
NM_001256169.2:c.189T= (APOM)	NP_001243098.1:p.Asn63=
NR_045828.2:n.446T= (APOM)