Canonical Allele Identifier: CA2677984127

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31657990-ACCCCATTACTATCAACTTTGCTTTTCTCCCTGGACTTCCCTTCTGTCCTTCTTTTTCCCTCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657997_31658058del , CM000668.2:g.31657997_31658058del	GRCh38
NC_000006.11:g.31625774_31625835del , CM000668.1:g.31625774_31625835del	GRCh37
NC_000006.10:g.31733753_31733814del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.542-67_542-6del (APOM) MANE Select	ENSP00000365081.3:n.542-67_542-6del
ENST00000375916.3:c.542-67_542-6del (APOM)	ENSP00000365081.3:n.542-67_542-6del
ENST00000375918.6:c.*209_*270del (APOM)	ENSP00000365083.2:n.*209_*270del
ENST00000375920.8:c.326-67_326-6del (APOM)	ENSP00000365085.4:n.326-67_326-6del
NM_001256169.1:c.326-67_326-6del (APOM)	NP_001243098.1:n.326-67_326-6del
NM_019101.2:c.542-67_542-6del (APOM)	NP_061974.2:n.542-67_542-6del
NR_045828.1:n.577-67_577-6del (APOM)
XM_006715150.2:c.446-67_446-6del (APOM)	XP_006715213.1:n.446-67_446-6del
XM_011514895.1:c.-14+2269_-14+2330del (BAG6)	XP_011513197.1:n.-14+2269_-14+2330del
XM_006715150.3:c.446-67_446-6del (APOM)	XP_006715213.1:n.446-67_446-6del
XM_017011279.2:c.-14+2269_-14+2330del (BAG6)	XP_016866768.1:n.-14+2269_-14+2330del
NM_019101.3:c.542-67_542-6del (APOM) MANE Select	NP_061974.2:n.542-67_542-6del
NM_001256169.2:c.326-67_326-6del (APOM)	NP_001243098.1:n.326-67_326-6del
NR_045828.2:n.583-67_583-6del (APOM)