Canonical Allele Identifier: CA487625230
Gene: SERPINA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.95085653G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94619316G>T , CM000676.2:g.94619316G>T GRCh38
NC_000014.8:g.95085653G>T , CM000676.1:g.95085653G>T GRCh37
NC_000014.7:g.94155406G>T NCBI36
NG_012879.1:g.11940G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000393078.5:c.765G>T MANE Select ENSP00000376793.3:p.Arg255=
ENST00000393078.4:c.765G>T ENSP00000376793.3:p.Arg255=
ENST00000393080.8:c.765G>T ENSP00000376795.4:p.Arg255=
ENST00000467132.5:c.765G>T ENSP00000450540.1:p.Arg255=
ENST00000482740.2:c.111G>T ENSP00000451119.1:p.Arg37=
ENST00000553947.1:c.1728G>T
ENST00000555820.1:c.765G>T ENSP00000452246.3:p.Arg255=
ENST00000556388.1:n.58-3025G>T
ENST00000556968.2:c.644-3025G>T ENSP00000452476.1:n.644-3025G>T
NM_001085.4:c.765G>T NP_001076.2:p.Arg255=
NM_001085.5:c.765G>T MANE Select NP_001076.2:p.Arg255=
NM_001384672.1:c.765G>T NP_001371601.1:p.Arg255=
NM_001384673.1:c.765G>T NP_001371602.1:p.Arg255=
NM_001384674.1:c.765G>T NP_001371603.1:p.Arg255=