Canonical Allele Identifier: CA487625300
Gene: SERPINA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.95085782G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94619445G>A , CM000676.2:g.94619445G>A GRCh38
NC_000014.8:g.95085782G>A , CM000676.1:g.95085782G>A GRCh37
NC_000014.7:g.94155535G>A NCBI36
NG_012879.1:g.12069G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393078.5:c.894G>A MANE Select ENSP00000376793.3:p.Arg298=
ENST00000393078.4:c.894G>A ENSP00000376793.3:p.Arg298=
ENST00000393080.8:c.894G>A ENSP00000376795.4:p.Arg298=
ENST00000467132.5:c.894G>A ENSP00000450540.1:p.Arg298=
ENST00000482740.2:c.240G>A ENSP00000451119.1:p.Arg80=
ENST00000553947.1:c.1857G>A
ENST00000555820.1:c.894G>A ENSP00000452246.3:p.Arg298=
ENST00000556388.1:n.58-2896G>A
ENST00000556968.2:c.644-2896G>A ENSP00000452476.1:n.644-2896G>A
ENST00000621603.1:c.113G>A
NM_001085.4:c.894G>A NP_001076.2:p.Arg298=
NM_001085.5:c.894G>A MANE Select NP_001076.2:p.Arg298=
NM_001384672.1:c.894G>A NP_001371601.1:p.Arg298=
NM_001384673.1:c.894G>A NP_001371602.1:p.Arg298=
NM_001384674.1:c.894G>A NP_001371603.1:p.Arg298=