Canonical Allele Identifier: CA2677983859

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657534-ACTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657538_31657540del , CM000668.2:g.31657538_31657540del	GRCh38
NC_000006.11:g.31625315_31625317del , CM000668.1:g.31625315_31625317del	GRCh37
NC_000006.10:g.31733294_31733296del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.442+60_442+62del (APOM) MANE Select	ENSP00000365081.3:n.442+60_442+62del
ENST00000375916.3:c.442+60_442+62del (APOM)	ENSP00000365081.3:n.442+60_442+62del
ENST00000375918.6:c.226+60_226+62del (APOM)	ENSP00000365083.2:n.226+60_226+62del
ENST00000375920.8:c.226+60_226+62del (APOM)	ENSP00000365085.4:n.226+60_226+62del
NM_001256169.1:c.226+60_226+62del (APOM)	NP_001243098.1:n.226+60_226+62del
NM_019101.2:c.442+60_442+62del (APOM)	NP_061974.2:n.442+60_442+62del
NR_045828.1:n.477+60_477+62del (APOM)
XM_006715150.2:c.346+60_346+62del (APOM)	XP_006715213.1:n.346+60_346+62del
XM_011514895.1:c.-14+2784_-14+2786del (BAG6)	XP_011513197.1:n.-14+2784_-14+2786del
XM_006715150.3:c.346+60_346+62del (APOM)	XP_006715213.1:n.346+60_346+62del
XM_017011279.2:c.-14+2784_-14+2786del (BAG6)	XP_016866768.1:n.-14+2784_-14+2786del
XM_024446545.1:c.-14+227_-14+229del (BAG6)	XP_024302313.1:n.-14+227_-14+229del
NM_019101.3:c.442+60_442+62del (APOM) MANE Select	NP_061974.2:n.442+60_442+62del
NM_001256169.2:c.226+60_226+62del (APOM)	NP_001243098.1:n.226+60_226+62del
NR_045828.2:n.483+60_483+62del (APOM)