Canonical Allele Identifier: CA1619250962

Gene: APOM BAG6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658037_31658040delinsCCTT , CM000668.2:g.31658037_31658040delinsCCTT	GRCh38
NC_000006.11:g.31625814_31625817delinsCCTT , CM000668.1:g.31625814_31625817delinsCCTT	GRCh37
NC_000006.10:g.31733793_31733796delinsCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.542-27_542-24delinsCCTT (APOM) MANE Select	ENSP00000365081.3:n.542-27_542-24delinsCCTT
ENST00000375916.3:c.542-27_542-24delinsCCTT (APOM)	ENSP00000365081.3:n.542-27_542-24delinsCCTT
ENST00000375918.6:c.*249_*252delinsCCTT (APOM)	ENSP00000365083.2:n.*249_*252delinsCCTT
ENST00000375920.8:c.326-27_326-24delinsCCTT (APOM)	ENSP00000365085.4:n.326-27_326-24delinsCCTT
NM_001256169.1:c.326-27_326-24delinsCCTT (APOM)	NP_001243098.1:n.326-27_326-24delinsCCTT
NM_019101.2:c.542-27_542-24delinsCCTT (APOM)	NP_061974.2:n.542-27_542-24delinsCCTT
NR_045828.1:n.577-27_577-24delinsCCTT (APOM)
XM_006715150.2:c.446-27_446-24delinsCCTT (APOM)	XP_006715213.1:n.446-27_446-24delinsCCTT
XM_011514895.1:c.-14+2281_-14+2284delinsAAGG (BAG6)	XP_011513197.1:n.-14+2281_-14+2284delinsAAGG
XM_006715150.3:c.446-27_446-24delinsCCTT (APOM)	XP_006715213.1:n.446-27_446-24delinsCCTT
XM_017011279.2:c.-14+2281_-14+2284delinsAAGG (BAG6)	XP_016866768.1:n.-14+2281_-14+2284delinsAAGG
NM_019101.3:c.542-27_542-24delinsCCTT (APOM) MANE Select	NP_061974.2:n.542-27_542-24delinsCCTT
NM_001256169.2:c.326-27_326-24delinsCCTT (APOM)	NP_001243098.1:n.326-27_326-24delinsCCTT
NR_045828.2:n.583-27_583-24delinsCCTT (APOM)