Canonical Allele Identifier: CA265884748

Gene: SERPINA3

Linked Data

• dbSNP Id: rs1032411799
• gnomAD v2: 14-95085548-C-T
• gnomAD v3: 14-94619211-C-T
• gnomAD v4: 14-94619211-C-T
• MyVariant Identifiers: chr14:g.95085548C>T (hg19) ; chr14:g.94619211C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94619211C>T , CM000676.2:g.94619211C>T	GRCh38
NC_000014.8:g.95085548C>T , CM000676.1:g.95085548C>T	GRCh37
NC_000014.7:g.94155301C>T	NCBI36
NG_012879.1:g.11835C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393078.5:c.660C>T MANE Select	ENSP00000376793.3:p.Pro220=
ENST00000393078.4:c.660C>T	ENSP00000376793.3:p.Pro220=
ENST00000393080.8:c.660C>T	ENSP00000376795.4:p.Pro220=
ENST00000467132.5:c.660C>T	ENSP00000450540.1:p.Pro220=
ENST00000482740.2:c.6C>T	ENSP00000451119.1:p.Pro2=
ENST00000553947.1:c.1623C>T
ENST00000555820.1:c.660C>T	ENSP00000452246.3:p.Pro220=
ENST00000556388.1:n.58-3130C>T
ENST00000556968.2:c.644-3130C>T	ENSP00000452476.1:n.644-3130C>T
NM_001085.4:c.660C>T	NP_001076.2:p.Pro220=
NM_001085.5:c.660C>T MANE Select	NP_001076.2:p.Pro220=
NM_001384672.1:c.660C>T	NP_001371601.1:p.Pro220=
NM_001384673.1:c.660C>T	NP_001371602.1:p.Pro220=
NM_001384674.1:c.660C>T	NP_001371603.1:p.Pro220=