Canonical Allele Identifier: CA1619250959

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658034_31658035delinsTG , CM000668.2:g.31658034_31658035delinsTG	GRCh38
NC_000006.11:g.31625811_31625812delinsTG , CM000668.1:g.31625811_31625812delinsTG	GRCh37
NC_000006.10:g.31733790_31733791delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.542-30_542-29delinsTG (APOM) MANE Select	ENSP00000365081.3:n.542-30_542-29delinsTG
ENST00000375916.3:c.542-30_542-29delinsTG (APOM)	ENSP00000365081.3:n.542-30_542-29delinsTG
ENST00000375918.6:c.*246_*247delinsTG (APOM)	ENSP00000365083.2:n.*246_*247delinsTG
ENST00000375920.8:c.326-30_326-29delinsTG (APOM)	ENSP00000365085.4:n.326-30_326-29delinsTG
NM_001256169.1:c.326-30_326-29delinsTG (APOM)	NP_001243098.1:n.326-30_326-29delinsTG
NM_019101.2:c.542-30_542-29delinsTG (APOM)	NP_061974.2:n.542-30_542-29delinsTG
NR_045828.1:n.577-30_577-29delinsTG (APOM)
XM_006715150.2:c.446-30_446-29delinsTG (APOM)	XP_006715213.1:n.446-30_446-29delinsTG
XM_011514895.1:c.-14+2286_-14+2287delinsCA (BAG6)	XP_011513197.1:n.-14+2286_-14+2287delinsCA
XM_006715150.3:c.446-30_446-29delinsTG (APOM)	XP_006715213.1:n.446-30_446-29delinsTG
XM_017011279.2:c.-14+2286_-14+2287delinsCA (BAG6)	XP_016866768.1:n.-14+2286_-14+2287delinsCA
NM_019101.3:c.542-30_542-29delinsTG (APOM) MANE Select	NP_061974.2:n.542-30_542-29delinsTG
NM_001256169.2:c.326-30_326-29delinsTG (APOM)	NP_001243098.1:n.326-30_326-29delinsTG
NR_045828.2:n.583-30_583-29delinsTG (APOM)