Canonical Allele Identifier: CA390856334

Gene: SERPINA3

Linked Data

• dbSNP Id: rs1267845120
• gnomAD v2: 14-95085783-T-C
• gnomAD v4: 14-94619446-T-C
• MyVariant Identifiers: chr14:g.95085783T>C (hg19) ; chr14:g.94619446T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94619446T>C , CM000676.2:g.94619446T>C	GRCh38
NC_000014.8:g.95085783T>C , CM000676.1:g.95085783T>C	GRCh37
NC_000014.7:g.94155536T>C	NCBI36
NG_012879.1:g.12070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393078.5:c.895T>C MANE Select	ENSP00000376793.3:p.Trp299Arg
ENST00000393078.4:c.895T>C	ENSP00000376793.3:p.Trp299Arg
ENST00000393080.8:c.895T>C	ENSP00000376795.4:p.Trp299Arg
ENST00000467132.5:c.895T>C	ENSP00000450540.1:p.Trp299Arg
ENST00000482740.2:c.241T>C	ENSP00000451119.1:p.Trp81Arg
ENST00000553947.1:c.1858T>C
ENST00000555820.1:c.895T>C	ENSP00000452246.3:p.Trp299Arg
ENST00000556388.1:n.58-2895T>C
ENST00000556968.2:c.644-2895T>C	ENSP00000452476.1:n.644-2895T>C
ENST00000621603.1:c.114T>C
NM_001085.4:c.895T>C	NP_001076.2:p.Trp299Arg
NM_001085.5:c.895T>C MANE Select	NP_001076.2:p.Trp299Arg
NM_001384672.1:c.895T>C	NP_001371601.1:p.Trp299Arg
NM_001384673.1:c.895T>C	NP_001371602.1:p.Trp299Arg
NM_001384674.1:c.895T>C	NP_001371603.1:p.Trp299Arg