Canonical Allele Identifier: CA1619250233

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656262_31656263delinsTG , CM000668.2:g.31656262_31656263delinsTG	GRCh38
NC_000006.11:g.31624039_31624040delinsTG , CM000668.1:g.31624039_31624040delinsTG	GRCh37
NC_000006.10:g.31732018_31732019delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.114+182_114+183delinsTG (APOM) MANE Select	ENSP00000365081.3:n.114+182_114+183delinsTG
ENST00000375916.3:c.114+182_114+183delinsTG (APOM)	ENSP00000365081.3:n.114+182_114+183delinsTG
ENST00000375918.6:c.-102-210_-102-209delinsTG (APOM)	ENSP00000365083.2:n.-102-210_-102-209delinsTG
ENST00000375920.8:c.-102-210_-102-209delinsTG (APOM)	ENSP00000365085.4:n.-102-210_-102-209delinsTG
NM_001256169.1:c.-102-210_-102-209delinsTG (APOM)	NP_001243098.1:n.-102-210_-102-209delinsTG
NM_019101.2:c.114+182_114+183delinsTG (APOM)	NP_061974.2:n.114+182_114+183delinsTG
NR_045828.1:n.143-210_143-209delinsTG (APOM)
XM_006715150.2:c.11+182_11+183delinsTG (APOM)	XP_006715213.1:n.11+182_11+183delinsTG
XM_011514895.1:c.-14+4058_-14+4059delinsCA (BAG6)	XP_011513197.1:n.-14+4058_-14+4059delinsCA
XM_006715150.3:c.11+182_11+183delinsTG (APOM)	XP_006715213.1:n.11+182_11+183delinsTG
XM_017011279.2:c.-14+4058_-14+4059delinsCA (BAG6)	XP_016866768.1:n.-14+4058_-14+4059delinsCA
XM_024446545.1:c.-14+1501_-14+1502delinsCA (BAG6)	XP_024302313.1:n.-14+1501_-14+1502delinsCA
NM_019101.3:c.114+182_114+183delinsTG (APOM) MANE Select	NP_061974.2:n.114+182_114+183delinsTG
NM_001256169.2:c.-102-210_-102-209delinsTG (APOM)	NP_001243098.1:n.-102-210_-102-209delinsTG
NR_045828.2:n.149-210_149-209delinsTG (APOM)