Canonical Allele Identifier: CA2155997686
Community Standard Title: NM_175739.4(SERPINA9):c.71C= (p.Ala24=)
Gene: SERPINA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94469770G= , CM000676.2:g.94469770G= GRCh38
NC_000014.8:g.94936107G= , CM000676.1:g.94936107G= GRCh37
NC_000014.7:g.94005860G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_175739.4:c.71C= MANE Select NP_783866.3:p.Ala24=
ENST00000674397.2:c.71C= MANE Select ENSP00000501517.1:p.Ala24=
NM_001042518.1:c.125C= NP_001035983.1:p.Ala42=
NM_001042518.2:c.71C= NP_001035983.2:p.Ala24=
NM_001284275.1:c.120-103C= NP_001271204.1:n.120-103C=
NM_001284275.2:c.-67-103C= NP_001271204.2:n.-67-103C=
NM_001284276.1:c.-19-304C= NP_001271205.1:n.-19-304C=
NM_001284276.2:c.-19-304C= NP_001271205.1:n.-19-304C=
NM_175739.3:c.125C= NP_783866.2:p.Ala42=
ENST00000298845.11:c.125C= ENSP00000298845.7:p.Ala42=
ENST00000298845.12:c.71C= ENSP00000298845.8:p.Ala24=
ENST00000337425.10:c.125C= ENSP00000337133.5:p.Ala42=
ENST00000337425.9:c.125C= ENSP00000337133.5:p.Ala42=
ENST00000380365.7:c.71C= ENSP00000369723.3:p.Ala24=
ENST00000424550.6:c.-19-304C= ENSP00000409012.2:n.-19-304C=
ENST00000448305.6:c.-67-103C= ENSP00000414092.2:n.-67-103C=
ENST00000538527.5:c.207C= ENSP00000441511.1:p.Gly69=
ENST00000539349.1:n.563C=
ENST00000546329.1:c.120-103C= ENSP00000445476.1:n.120-103C=
ENST00000546329.2:c.-67-103C= ENSP00000445476.2:n.-67-103C=
ENST00000674164.1:c.125C= ENSP00000501328.1:p.Ala42=
XM_011536713.1:c.71C= XP_011535015.1:p.Ala24=
XM_011536714.1:c.71C= XP_011535016.1:p.Ala24=
XM_011536714.2:c.71C= XP_011535016.1:p.Ala24=
XM_011536715.1:c.71C= XP_011535017.1:p.Ala24=
XM_011536715.2:c.71C= XP_011535017.1:p.Ala24=
XM_011536716.1:c.-67-103C= XP_011535018.1:n.-67-103C=
XM_011536716.2:c.-67-103C= XP_011535018.1:n.-67-103C=
XM_011536717.1:c.-67-103C= XP_011535019.1:n.-67-103C=