Canonical Allele Identifier: CA2677983511

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657158-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657158_31657159insC , CM000668.2:g.31657158_31657159insC	GRCh38
NC_000006.11:g.31624935_31624936insC , CM000668.1:g.31624935_31624936insC	GRCh37
NC_000006.10:g.31732914_31732915insC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375916.4:c.270-67_270-66insC (APOM) MANE Select	ENSP00000365081.3:n.270-67_270-66insC
ENST00000375916.3:c.270-67_270-66insC (APOM)	ENSP00000365081.3:n.270-67_270-66insC
ENST00000375918.6:c.54-67_54-66insC (APOM)	ENSP00000365083.2:n.54-67_54-66insC
ENST00000375920.8:c.54-67_54-66insC (APOM)	ENSP00000365085.4:n.54-67_54-66insC
NM_001256169.1:c.54-67_54-66insC (APOM)	NP_001243098.1:n.54-67_54-66insC
NM_019101.2:c.270-67_270-66insC (APOM)	NP_061974.2:n.270-67_270-66insC
NR_045828.1:n.305-67_305-66insC (APOM)
XM_006715150.2:c.174-67_174-66insC (APOM)	XP_006715213.1:n.174-67_174-66insC
XM_011514895.1:c.-14+3162_-14+3163insG (BAG6)	XP_011513197.1:n.-14+3162_-14+3163insG
XM_006715150.3:c.174-67_174-66insC (APOM)	XP_006715213.1:n.174-67_174-66insC
XM_017011279.2:c.-14+3162_-14+3163insG (BAG6)	XP_016866768.1:n.-14+3162_-14+3163insG
XM_024446545.1:c.-14+605_-14+606insG (BAG6)	XP_024302313.1:n.-14+605_-14+606insG
NM_019101.3:c.270-67_270-66insC (APOM) MANE Select	NP_061974.2:n.270-67_270-66insC
NM_001256169.2:c.54-67_54-66insC (APOM)	NP_001243098.1:n.54-67_54-66insC
NR_045828.2:n.311-67_311-66insC (APOM)