Canonical Allele Identifier: CA8274713

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1771878G>A , CM000679.2:g.1771878G>A	GRCh38
NC_000017.10:g.1675172G>A , CM000679.1:g.1675172G>A	GRCh37
NC_000017.9:g.1621922G>A	NCBI36
NG_028180.1:g.14914G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.446G>A MANE Select	NP_002606.3:p.Arg149His
ENST00000254722.9:c.446G>A MANE Select	ENSP00000254722.4:p.Arg149His
NM_001329903.1:c.446G>A	NP_001316832.1:p.Arg149His
NM_001329903.2:c.446G>A	NP_001316832.1:p.Arg149His
NM_001329904.1:c.-116G>A	NP_001316833.1:n.-116G>A
NM_001329904.2:c.-116G>A	NP_001316833.1:n.-116G>A
NM_001329905.1:c.-116G>A	NP_001316834.1:n.-116G>A
NM_001329905.2:c.-116G>A	NP_001316834.1:n.-116G>A
NM_002615.5:c.446G>A	NP_002606.3:p.Arg149His
NM_002615.6:c.446G>A	NP_002606.3:p.Arg149His
ENST00000254722.8:c.446G>A	ENSP00000254722.4:p.Arg149His
ENST00000570820.1:n.666G>A
ENST00000571870.5:n.687G>A
ENST00000572048.1:c.-116G>A	ENSP00000458484.1:n.-116G>A
ENST00000573763.1:c.-156G>A	ENSP00000461405.1:n.-156G>A
ENST00000573770.5:c.*296G>A	ENSP00000459107.1:n.*296G>A
ENST00000576406.5:c.-116G>A	ENSP00000461214.1:n.-116G>A