Canonical Allele Identifier: CA1619250308

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31656455_31656459delinsCTTCA , CM000668.2:g.31656455_31656459delinsCTTCA	GRCh38
NC_000006.11:g.31624232_31624236delinsCTTCA , CM000668.1:g.31624232_31624236delinsCTTCA	GRCh37
NC_000006.10:g.31732211_31732215delinsCTTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.115-17_115-13delinsCTTCA (APOM) MANE Select	ENSP00000365081.3:n.115-17_115-13delinsCTTCA
ENST00000375916.3:c.115-17_115-13delinsCTTCA (APOM)	ENSP00000365081.3:n.115-17_115-13delinsCTTCA
ENST00000375918.6:c.-102-17_-102-13delinsCTTCA (APOM)	ENSP00000365083.2:n.-102-17_-102-13delinsCTTCA
ENST00000375920.8:c.-102-17_-102-13delinsCTTCA (APOM)	ENSP00000365085.4:n.-102-17_-102-13delinsCTTCA
NM_001256169.1:c.-102-17_-102-13delinsCTTCA (APOM)	NP_001243098.1:n.-102-17_-102-13delinsCTTCA
NM_019101.2:c.115-17_115-13delinsCTTCA (APOM)	NP_061974.2:n.115-17_115-13delinsCTTCA
NR_045828.1:n.143-17_143-13delinsCTTCA (APOM)
XM_006715150.2:c.12-17_12-13delinsCTTCA (APOM)	XP_006715213.1:n.12-17_12-13delinsCTTCA
XM_011514895.1:c.-14+3862_-14+3866delinsTGAAG (BAG6)	XP_011513197.1:n.-14+3862_-14+3866delinsTGAAG
XM_006715150.3:c.12-17_12-13delinsCTTCA (APOM)	XP_006715213.1:n.12-17_12-13delinsCTTCA
XM_017011279.2:c.-14+3862_-14+3866delinsTGAAG (BAG6)	XP_016866768.1:n.-14+3862_-14+3866delinsTGAAG
XM_024446545.1:c.-14+1305_-14+1309delinsTGAAG (BAG6)	XP_024302313.1:n.-14+1305_-14+1309delinsTGAAG
NM_019101.3:c.115-17_115-13delinsCTTCA (APOM) MANE Select	NP_061974.2:n.115-17_115-13delinsCTTCA
NM_001256169.2:c.-102-17_-102-13delinsCTTCA (APOM)	NP_001243098.1:n.-102-17_-102-13delinsCTTCA
NR_045828.2:n.149-17_149-13delinsCTTCA (APOM)