Canonical Allele Identifier: CA2677982196

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31655692-G-GCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31655693_31655694insCTGTC , CM000668.2:g.31655693_31655694insCTGTC	GRCh38
NC_000006.11:g.31623470_31623471insCTGTC , CM000668.1:g.31623470_31623471insCTGTC	GRCh37
NC_000006.10:g.31731449_31731450insCTGTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.3:c.-274_-273insCTGTC (APOM)	ENSP00000365081.3:n.-274_-273insCTGTC
ENST00000375918.6:c.-102-779_-102-778insCTGTC (APOM)	ENSP00000365083.2:n.-102-779_-102-778insCTGTC
ENST00000375920.8:c.-102-779_-102-778insCTGTC (APOM)	ENSP00000365085.4:n.-102-779_-102-778insCTGTC
NM_001256169.1:c.-102-779_-102-778insCTGTC (APOM)	NP_001243098.1:n.-102-779_-102-778insCTGTC
NR_045828.1:n.143-779_143-778insCTGTC (APOM)
XM_006715150.2:c.-377_-376insCTGTC (APOM)	XP_006715213.1:n.-377_-376insCTGTC
XM_011514895.1:c.-13-3917_-13-3916insACAGG (BAG6)	XP_011513197.1:n.-13-3917_-13-3916insACAGG
XM_017011279.2:c.-13-3917_-13-3916insACAGG (BAG6)	XP_016866768.1:n.-13-3917_-13-3916insACAGG
XM_024446545.1:c.-14+2071_-14+2072insACAGG (BAG6)	XP_024302313.1:n.-14+2071_-14+2072insACAGG
NM_001256169.2:c.-102-779_-102-778insCTGTC (APOM)	NP_001243098.1:n.-102-779_-102-778insCTGTC
NR_045828.2:n.149-779_149-778insCTGTC (APOM)