Canonical Allele Identifier: CA823895244

Gene: APOM BAG6

Linked Data

• dbSNP Id: rs1315731124
• gnomAD v3: 6-31657155-A-AG
• gnomAD v4: 6-31657155-A-AG
• MyVariant Identifiers: chr6:g.31624932_31624933insG (hg19) ; chr6:g.31657155_31657156insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657155_31657156insG , CM000668.2:g.31657155_31657156insG	GRCh38
NC_000006.11:g.31624932_31624933insG , CM000668.1:g.31624932_31624933insG	GRCh37
NC_000006.10:g.31732911_31732912insG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-70_270-69insG (APOM) MANE Select	ENSP00000365081.3:n.270-70_270-69insG
ENST00000375916.3:c.270-70_270-69insG (APOM)	ENSP00000365081.3:n.270-70_270-69insG
ENST00000375918.6:c.54-70_54-69insG (APOM)	ENSP00000365083.2:n.54-70_54-69insG
ENST00000375920.8:c.54-70_54-69insG (APOM)	ENSP00000365085.4:n.54-70_54-69insG
NM_001256169.1:c.54-70_54-69insG (APOM)	NP_001243098.1:n.54-70_54-69insG
NM_019101.2:c.270-70_270-69insG (APOM)	NP_061974.2:n.270-70_270-69insG
NR_045828.1:n.305-70_305-69insG (APOM)
XM_006715150.2:c.174-70_174-69insG (APOM)	XP_006715213.1:n.174-70_174-69insG
XM_011514895.1:c.-14+3165_-14+3166insC (BAG6)	XP_011513197.1:n.-14+3165_-14+3166insC
XM_006715150.3:c.174-70_174-69insG (APOM)	XP_006715213.1:n.174-70_174-69insG
XM_017011279.2:c.-14+3165_-14+3166insC (BAG6)	XP_016866768.1:n.-14+3165_-14+3166insC
XM_024446545.1:c.-14+608_-14+609insC (BAG6)	XP_024302313.1:n.-14+608_-14+609insC
NM_019101.3:c.270-70_270-69insG (APOM) MANE Select	NP_061974.2:n.270-70_270-69insG
NM_001256169.2:c.54-70_54-69insG (APOM)	NP_001243098.1:n.54-70_54-69insG
NR_045828.2:n.311-70_311-69insG (APOM)