Canonical Allele Identifier: CA2243024039

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1771040C= , CM000679.2:g.1771040C=	GRCh38
NC_000017.10:g.1674334C= , CM000679.1:g.1674334C=	GRCh37
NC_000017.9:g.1621084C=	NCBI36
NG_028180.1:g.14076C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.295C= MANE Select	NP_002606.3:p.Arg99=
ENST00000254722.9:c.295C= MANE Select	ENSP00000254722.4:p.Arg99=
NM_001329903.1:c.295C=	NP_001316832.1:p.Arg99=
NM_001329903.2:c.295C=	NP_001316832.1:p.Arg99=
NM_001329904.1:c.-267C=	NP_001316833.1:n.-267C=
NM_001329904.2:c.-267C=	NP_001316833.1:n.-267C=
NM_002615.5:c.295C=	NP_002606.3:p.Arg99=
NM_002615.6:c.295C=	NP_002606.3:p.Arg99=
ENST00000254722.8:c.295C=	ENSP00000254722.4:p.Arg99=
ENST00000570731.5:c.295C=	ENSP00000459869.1:p.Arg99=
ENST00000570820.1:n.515C=
ENST00000571360.5:c.256C=	ENSP00000461660.1:p.Arg86=
ENST00000571870.5:n.536C=
ENST00000573770.5:c.*145C=	ENSP00000459107.1:n.*145C=
ENST00000576406.5:c.-267C=	ENSP00000461214.1:n.-267C=
ENST00000577053.1:c.295C=	ENSP00000460842.1:p.Arg99=