Canonical Allele Identifier: CA390856354

Gene: SERPINA3

Linked Data

• dbSNP Id: rs2139961120
• gnomAD v4: 14-94619450-G-T
• MyVariant Identifiers: chr14:g.95085787G>T (hg19) ; chr14:g.94619450G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94619450G>T , CM000676.2:g.94619450G>T	GRCh38
NC_000014.8:g.95085787G>T , CM000676.1:g.95085787G>T	GRCh37
NC_000014.7:g.94155540G>T	NCBI36
NG_012879.1:g.12074G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393078.5:c.899G>T MANE Select	ENSP00000376793.3:p.Arg300Ile
ENST00000393078.4:c.899G>T	ENSP00000376793.3:p.Arg300Ile
ENST00000393080.8:c.899G>T	ENSP00000376795.4:p.Arg300Ile
ENST00000467132.5:c.899G>T	ENSP00000450540.1:p.Arg300Ile
ENST00000482740.2:c.245G>T	ENSP00000451119.1:p.Arg82Ile
ENST00000553947.1:c.1862G>T
ENST00000555820.1:c.899G>T	ENSP00000452246.3:p.Arg300Ile
ENST00000556388.1:n.58-2891G>T
ENST00000556968.2:c.644-2891G>T	ENSP00000452476.1:n.644-2891G>T
ENST00000621603.1:c.118G>T
NM_001085.4:c.899G>T	NP_001076.2:p.Arg300Ile
NM_001085.5:c.899G>T MANE Select	NP_001076.2:p.Arg300Ile
NM_001384672.1:c.899G>T	NP_001371601.1:p.Arg300Ile
NM_001384673.1:c.899G>T	NP_001371602.1:p.Arg300Ile
NM_001384674.1:c.899G>T	NP_001371603.1:p.Arg300Ile