Canonical Allele Identifier: CA2677984292
Gene: APOM HGNC NCBI
BAG6 HGNC NCBI

Linked Data

gnomAD v4: 6-31658160-T-TTCCAGC
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658170_31658175dup , CM000668.2:g.31658170_31658175dup GRCh38
NC_000006.11:g.31625947_31625952dup , CM000668.1:g.31625947_31625952dup GRCh37
NC_000006.10:g.31733926_31733931dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.*81_*86dup (APOM) MANE Select ENSP00000365081.3:n.*81_*86dup
ENST00000375916.3:c.*81_*86dup (APOM) ENSP00000365081.3:n.*81_*86dup
ENST00000375920.8:c.*81_*86dup (APOM) ENSP00000365085.4:n.*81_*86dup
NM_001256169.1:c.*81_*86dup (APOM) NP_001243098.1:n.*81_*86dup
NM_019101.2:c.*81_*86dup (APOM) NP_061974.2:n.*81_*86dup
NR_045828.1:n.683_688dup (APOM)
XM_006715150.2:c.*81_*86dup (APOM) XP_006715213.1:n.*81_*86dup
XM_011514895.1:c.-14+2155_-14+2160dup (BAG6) XP_011513197.1:n.-14+2155_-14+2160dup
XM_006715150.3:c.*81_*86dup (APOM) XP_006715213.1:n.*81_*86dup
XM_017011279.2:c.-14+2155_-14+2160dup (BAG6) XP_016866768.1:n.-14+2155_-14+2160dup
NM_019101.3:c.*81_*86dup (APOM) MANE Select NP_061974.2:n.*81_*86dup
NM_001256169.2:c.*81_*86dup (APOM) NP_001243098.1:n.*81_*86dup
NR_045828.2:n.689_694dup (APOM)
Search 100 bp 5'
Search 100 bp 3'