Canonical Allele Identifier: CA487625297
Gene: SERPINA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.95085776G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94619439G>C , CM000676.2:g.94619439G>C GRCh38
NC_000014.8:g.95085776G>C , CM000676.1:g.95085776G>C GRCh37
NC_000014.7:g.94155529G>C NCBI36
NG_012879.1:g.12063G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393078.5:c.888G>C MANE Select ENSP00000376793.3:p.Leu296=
ENST00000393078.4:c.888G>C ENSP00000376793.3:p.Leu296=
ENST00000393080.8:c.888G>C ENSP00000376795.4:p.Leu296=
ENST00000467132.5:c.888G>C ENSP00000450540.1:p.Leu296=
ENST00000482740.2:c.234G>C ENSP00000451119.1:p.Leu78=
ENST00000553947.1:c.1851G>C
ENST00000555820.1:c.888G>C ENSP00000452246.3:p.Leu296=
ENST00000556388.1:n.58-2902G>C
ENST00000556968.2:c.644-2902G>C ENSP00000452476.1:n.644-2902G>C
ENST00000621603.1:c.107G>C
NM_001085.4:c.888G>C NP_001076.2:p.Leu296=
NM_001085.5:c.888G>C MANE Select NP_001076.2:p.Leu296=
NM_001384672.1:c.888G>C NP_001371601.1:p.Leu296=
NM_001384673.1:c.888G>C NP_001371602.1:p.Leu296=
NM_001384674.1:c.888G>C NP_001371603.1:p.Leu296=