Canonical Allele Identifier: CA2243025997
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1772012A= , CM000679.2:g.1772012A= GRCh38
NC_000017.10:g.1675306A= , CM000679.1:g.1675306A= GRCh37
NC_000017.9:g.1622056A= NCBI36
NG_028180.1:g.15048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254722.9:c.580A= MANE Select ENSP00000254722.4:p.Arg194=
ENST00000254722.8:c.580A= ENSP00000254722.4:p.Arg194=
ENST00000570820.1:n.800A=
ENST00000572048.1:c.19A= ENSP00000458484.1:p.Arg7=
ENST00000573763.1:c.-22A= ENSP00000461405.1:n.-22A=
ENST00000576406.5:c.19A= ENSP00000461214.1:p.Arg7=
NM_002615.5:c.580A= NP_002606.3:p.Arg194=
NM_001329903.1:c.580A= NP_001316832.1:p.Arg194=
NM_001329904.1:c.19A= NP_001316833.1:p.Arg7=
NM_001329905.1:c.19A= NP_001316834.1:p.Arg7=
NM_002615.6:c.580A= NP_002606.3:p.Arg194=
NM_002615.7:c.580A= MANE Select NP_002606.3:p.Arg194=
NM_001329903.2:c.580A= NP_001316832.1:p.Arg194=
NM_001329904.2:c.19A= NP_001316833.1:p.Arg7=
NM_001329905.2:c.19A= NP_001316834.1:p.Arg7=