Canonical Allele Identifier: CA363427006

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657253T>C , CM000668.2:g.31657253T>C GRCh38
NC_000006.11:g.31625030T>C , CM000668.1:g.31625030T>C GRCh37
NC_000006.10:g.31733009T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.298T>C (APOM) MANE Select ENSP00000365081.3:p.Trp100Arg
ENST00000375916.3:c.298T>C (APOM) ENSP00000365081.3:p.Trp100Arg
ENST00000375918.6:c.82T>C (APOM) ENSP00000365083.2:p.Trp28Arg
ENST00000375920.8:c.82T>C (APOM) ENSP00000365085.4:p.Trp28Arg
NM_001256169.1:c.82T>C (APOM) NP_001243098.1:p.Trp28Arg
NM_019101.2:c.298T>C (APOM) NP_061974.2:p.Trp100Arg
NR_045828.1:n.333T>C (APOM)
XM_006715150.2:c.202T>C (APOM) XP_006715213.1:p.Trp68Arg
XM_011514895.1:c.-14+3068A>G (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.202T>C (APOM) XP_006715213.1:p.Trp68Arg
XM_017011279.2:c.-14+3068A>G (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+511A>G (BAG6) XP_024302313.1:p.=
NM_019101.3:c.298T>C (APOM) MANE Select NP_061974.2:p.Trp100Arg
NM_001256169.2:c.82T>C (APOM) NP_001243098.1:p.Trp28Arg
NR_045828.2:n.339T>C (APOM)