Canonical Allele Identifier: CA2985885064

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657234dup , CM000668.2:g.31657234dup	GRCh38
NC_000006.11:g.31625011dup , CM000668.1:g.31625011dup	GRCh37
NC_000006.10:g.31732990dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.279dup (APOM) MANE Select	ENSP00000365081.3:p.Leu94AlafsTer13
ENST00000375916.3:c.279dup (APOM)	ENSP00000365081.3:p.Leu94AlafsTer13
ENST00000375918.6:c.63dup (APOM)	ENSP00000365083.2:p.Leu22AlafsTer13
ENST00000375920.8:c.63dup (APOM)	ENSP00000365085.4:p.Leu22AlafsTer13
NM_001256169.1:c.63dup (APOM)	NP_001243098.1:p.Leu22AlafsTer13
NM_019101.2:c.279dup (APOM)	NP_061974.2:p.Leu94AlafsTer13
NR_045828.1:n.314dup (APOM)
XM_006715150.2:c.183dup (APOM)	XP_006715213.1:p.Leu62AlafsTer13
XM_011514895.1:c.-14+3089dup (BAG6)	XP_011513197.1:n.-14+3089dup
XM_006715150.3:c.183dup (APOM)	XP_006715213.1:p.Leu62AlafsTer13
XM_017011279.2:c.-14+3089dup (BAG6)	XP_016866768.1:n.-14+3089dup
XM_024446545.1:c.-14+532dup (BAG6)	XP_024302313.1:n.-14+532dup
NM_019101.3:c.279dup (APOM) MANE Select	NP_061974.2:p.Leu94AlafsTer13
NM_001256169.2:c.63dup (APOM)	NP_001243098.1:p.Leu22AlafsTer13
NR_045828.2:n.320dup (APOM)