Canonical Allele Identifier: CA390856261

Gene: SERPINA3

Linked Data

• MyVariant Identifiers: chr14:g.95085765C>A (hg19) ; chr14:g.94619428C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94619428C>A , CM000676.2:g.94619428C>A	GRCh38
NC_000014.8:g.95085765C>A , CM000676.1:g.95085765C>A	GRCh37
NC_000014.7:g.94155518C>A	NCBI36
NG_012879.1:g.12052C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393078.5:c.877C>A MANE Select	ENSP00000376793.3:p.Pro293Thr
ENST00000393078.4:c.877C>A	ENSP00000376793.3:p.Pro293Thr
ENST00000393080.8:c.877C>A	ENSP00000376795.4:p.Pro293Thr
ENST00000467132.5:c.877C>A	ENSP00000450540.1:p.Pro293Thr
ENST00000482740.2:c.223C>A	ENSP00000451119.1:p.Pro75Thr
ENST00000553947.1:c.1840C>A
ENST00000555820.1:c.877C>A	ENSP00000452246.3:p.Pro293Thr
ENST00000556388.1:n.58-2913C>A
ENST00000556968.2:c.644-2913C>A	ENSP00000452476.1:n.644-2913C>A
ENST00000621603.1:c.96C>A
NM_001085.4:c.877C>A	NP_001076.2:p.Pro293Thr
NM_001085.5:c.877C>A MANE Select	NP_001076.2:p.Pro293Thr
NM_001384672.1:c.877C>A	NP_001371601.1:p.Pro293Thr
NM_001384673.1:c.877C>A	NP_001371602.1:p.Pro293Thr
NM_001384674.1:c.877C>A	NP_001371603.1:p.Pro293Thr