Canonical Allele Identifier: CA2677984293

Gene: APOM BAG6

Linked Data

• gnomAD v4: 6-31658160-TTCCAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31658170_31658175del , CM000668.2:g.31658170_31658175del	GRCh38
NC_000006.11:g.31625947_31625952del , CM000668.1:g.31625947_31625952del	GRCh37
NC_000006.10:g.31733926_31733931del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.*81_*86del (APOM) MANE Select	ENSP00000365081.3:n.*81_*86del
ENST00000375916.3:c.*81_*86del (APOM)	ENSP00000365081.3:n.*81_*86del
ENST00000375920.8:c.*81_*86del (APOM)	ENSP00000365085.4:n.*81_*86del
NM_001256169.1:c.*81_*86del (APOM)	NP_001243098.1:n.*81_*86del
NM_019101.2:c.*81_*86del (APOM)	NP_061974.2:n.*81_*86del
NR_045828.1:n.683_688del (APOM)
XM_006715150.2:c.*81_*86del (APOM)	XP_006715213.1:n.*81_*86del
XM_011514895.1:c.-14+2155_-14+2160del (BAG6)	XP_011513197.1:n.-14+2155_-14+2160del
XM_006715150.3:c.*81_*86del (APOM)	XP_006715213.1:n.*81_*86del
XM_017011279.2:c.-14+2155_-14+2160del (BAG6)	XP_016866768.1:n.-14+2155_-14+2160del
NM_019101.3:c.*81_*86del (APOM) MANE Select	NP_061974.2:n.*81_*86del
NM_001256169.2:c.*81_*86del (APOM)	NP_001243098.1:n.*81_*86del
NR_045828.2:n.689_694del (APOM)