Canonical Allele Identifier: CA2156056583
Gene: SERPINA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94587410G= , CM000676.2:g.94587410G= GRCh38
NC_000014.8:g.95053747G= , CM000676.1:g.95053747G= GRCh37
NC_000014.7:g.94123500G= NCBI36
NG_032908.2:g.30969G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329597.12:c.48G= MANE Select ENSP00000333203.7:p.Gly16=
ENST00000329597.11:c.48G= ENSP00000333203.7:p.Gly16=
ENST00000553511.1:c.48G= ENSP00000451215.1:p.Gly16=
ENST00000553780.5:c.48G= ENSP00000450837.1:p.Gly16=
ENST00000554220.5:c.48G= ENSP00000450484.1:p.Gly16=
ENST00000554276.1:c.48G= ENSP00000451610.1:p.Gly16=
ENST00000554633.5:c.48G= ENSP00000451697.1:p.Gly16=
ENST00000554760.5:c.48G= ENSP00000452469.1:p.Gly16=
ENST00000554866.5:c.48G= ENSP00000451126.1:p.Gly16=
ENST00000555681.1:c.48G= ENSP00000451650.1:p.Gly16=
ENST00000556064.1:c.48G= ENSP00000451487.1:p.Gly16=
ENST00000556730.1:n.165G=
ENST00000556775.5:c.48G= ENSP00000450745.1:p.Gly16=
ENST00000557598.1:c.48G= ENSP00000450485.1:p.Gly16=
NM_000624.5:c.48G= NP_000615.3:p.Gly16=
NM_000624.6:c.48G= MANE Select NP_000615.3:p.Gly16=