Canonical Allele Identifier: CA2839262002

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657152A>G , CM000668.2:g.31657152A>G	GRCh38
NC_000006.11:g.31624929A>G , CM000668.1:g.31624929A>G	GRCh37
NC_000006.10:g.31732908A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.270-73A>G (APOM) MANE Select	ENSP00000365081.3:n.270-73A>G
ENST00000375916.3:c.270-73A>G (APOM)	ENSP00000365081.3:n.270-73A>G
ENST00000375918.6:c.54-73A>G (APOM)	ENSP00000365083.2:n.54-73A>G
ENST00000375920.8:c.54-73A>G (APOM)	ENSP00000365085.4:n.54-73A>G
NM_001256169.1:c.54-73A>G (APOM)	NP_001243098.1:n.54-73A>G
NM_019101.2:c.270-73A>G (APOM)	NP_061974.2:n.270-73A>G
NR_045828.1:n.305-73A>G (APOM)
XM_006715150.2:c.174-73A>G (APOM)	XP_006715213.1:n.174-73A>G
XM_011514895.1:c.-14+3169T>C (BAG6)	XP_011513197.1:n.-14+3169T>C
XM_006715150.3:c.174-73A>G (APOM)	XP_006715213.1:n.174-73A>G
XM_017011279.2:c.-14+3169T>C (BAG6)	XP_016866768.1:n.-14+3169T>C
XM_024446545.1:c.-14+612T>C (BAG6)	XP_024302313.1:n.-14+612T>C
NM_019101.3:c.270-73A>G (APOM) MANE Select	NP_061974.2:n.270-73A>G
NM_001256169.2:c.54-73A>G (APOM)	NP_001243098.1:n.54-73A>G
NR_045828.2:n.311-73A>G (APOM)