Canonical Allele Identifier: CA363431586

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625846T>A (hg19) ; chr6:g.31658069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658069T>A , CM000668.2:g.31658069T>A	GRCh38
NC_000006.11:g.31625846T>A , CM000668.1:g.31625846T>A	GRCh37
NC_000006.10:g.31733825T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.547T>A (APOM) MANE Select	ENSP00000365081.3:p.Cys183Ser
ENST00000375916.3:c.547T>A (APOM)	ENSP00000365081.3:p.Cys183Ser
ENST00000375918.6:c.*281T>A (APOM)	ENSP00000365083.2:n.*281T>A
ENST00000375920.8:c.331T>A (APOM)	ENSP00000365085.4:p.Cys111Ser
NM_001256169.1:c.331T>A (APOM)	NP_001243098.1:p.Cys111Ser
NM_019101.2:c.547T>A (APOM)	NP_061974.2:p.Cys183Ser
NR_045828.1:n.582T>A (APOM)
XM_006715150.2:c.451T>A (APOM)	XP_006715213.1:p.Cys151Ser
XM_011514895.1:c.-14+2252A>T (BAG6)	XP_011513197.1:n.-14+2252A>T
XM_006715150.3:c.451T>A (APOM)	XP_006715213.1:p.Cys151Ser
XM_017011279.2:c.-14+2252A>T (BAG6)	XP_016866768.1:n.-14+2252A>T
NM_019101.3:c.547T>A (APOM) MANE Select	NP_061974.2:p.Cys183Ser
NM_001256169.2:c.331T>A (APOM)	NP_001243098.1:p.Cys111Ser
NR_045828.2:n.588T>A (APOM)