Canonical Allele Identifier: CA449667031

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625200A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657423A>C , CM000668.2:g.31657423A>C	GRCh38
NC_000006.11:g.31625200A>C , CM000668.1:g.31625200A>C	GRCh37
NC_000006.10:g.31733179A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.387A>C (APOM) MANE Select	ENSP00000365081.3:p.Pro129=
ENST00000375916.3:c.387A>C (APOM)	ENSP00000365081.3:p.Pro129=
ENST00000375918.6:c.171A>C (APOM)	ENSP00000365083.2:p.Pro57=
ENST00000375920.8:c.171A>C (APOM)	ENSP00000365085.4:p.Pro57=
NM_001256169.1:c.171A>C (APOM)	NP_001243098.1:p.Pro57=
NM_019101.2:c.387A>C (APOM)	NP_061974.2:p.Pro129=
NR_045828.1:n.422A>C (APOM)
XM_006715150.2:c.291A>C (APOM)	XP_006715213.1:p.Pro97=
XM_011514895.1:c.-14+2898T>G (BAG6)	XP_011513197.1:n.-14+2898T>G
XM_006715150.3:c.291A>C (APOM)	XP_006715213.1:p.Pro97=
XM_017011279.2:c.-14+2898T>G (BAG6)	XP_016866768.1:n.-14+2898T>G
XM_024446545.1:c.-14+341T>G (BAG6)	XP_024302313.1:n.-14+341T>G
NM_019101.3:c.387A>C (APOM) MANE Select	NP_061974.2:p.Pro129=
NM_001256169.2:c.171A>C (APOM)	NP_001243098.1:p.Pro57=
NR_045828.2:n.428A>C (APOM)