Canonical Allele Identifier: CA2677983474

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657145-C-CAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657154_31657159dup , CM000668.2:g.31657154_31657159dup	GRCh38
NC_000006.11:g.31624931_31624936dup , CM000668.1:g.31624931_31624936dup	GRCh37
NC_000006.10:g.31732910_31732915dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-71_270-66dup (APOM) MANE Select	ENSP00000365081.3:n.270-71_270-66dup
ENST00000375916.3:c.270-71_270-66dup (APOM)	ENSP00000365081.3:n.270-71_270-66dup
ENST00000375918.6:c.54-71_54-66dup (APOM)	ENSP00000365083.2:n.54-71_54-66dup
ENST00000375920.8:c.54-71_54-66dup (APOM)	ENSP00000365085.4:n.54-71_54-66dup
NM_001256169.1:c.54-71_54-66dup (APOM)	NP_001243098.1:n.54-71_54-66dup
NM_019101.2:c.270-71_270-66dup (APOM)	NP_061974.2:n.270-71_270-66dup
NR_045828.1:n.305-71_305-66dup (APOM)
XM_006715150.2:c.174-71_174-66dup (APOM)	XP_006715213.1:n.174-71_174-66dup
XM_011514895.1:c.-14+3170_-14+3175dup (BAG6)	XP_011513197.1:n.-14+3170_-14+3175dup
XM_006715150.3:c.174-71_174-66dup (APOM)	XP_006715213.1:n.174-71_174-66dup
XM_017011279.2:c.-14+3170_-14+3175dup (BAG6)	XP_016866768.1:n.-14+3170_-14+3175dup
XM_024446545.1:c.-14+613_-14+618dup (BAG6)	XP_024302313.1:n.-14+613_-14+618dup
NM_019101.3:c.270-71_270-66dup (APOM) MANE Select	NP_061974.2:n.270-71_270-66dup
NM_001256169.2:c.54-71_54-66dup (APOM)	NP_001243098.1:n.54-71_54-66dup
NR_045828.2:n.311-71_311-66dup (APOM)