Canonical Allele Identifier: CA2243022137

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1769982C= , CM000679.2:g.1769982C=	GRCh38
NC_000017.10:g.1673276C= , CM000679.1:g.1673276C=	GRCh37
NC_000017.9:g.1620026C=	NCBI36
NG_028180.1:g.13018C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.215C= MANE Select	NP_002606.3:p.Thr72=
ENST00000254722.9:c.215C= MANE Select	ENSP00000254722.4:p.Thr72=
NM_001329903.1:c.215C=	NP_001316832.1:p.Thr72=
NM_001329903.2:c.215C=	NP_001316832.1:p.Thr72=
NM_001329904.1:c.-347C=	NP_001316833.1:n.-347C=
NM_001329904.2:c.-347C=	NP_001316833.1:n.-347C=
NM_002615.5:c.215C=	NP_002606.3:p.Thr72=
NM_002615.6:c.215C=	NP_002606.3:p.Thr72=
ENST00000254722.8:c.215C=	ENSP00000254722.4:p.Thr72=
ENST00000570731.5:c.215C=	ENSP00000459869.1:p.Thr72=
ENST00000571149.5:c.215C=	ENSP00000460905.1:p.Thr72=
ENST00000571360.5:c.176C=	ENSP00000461660.1:p.Thr59=
ENST00000571870.5:n.456C=
ENST00000573770.5:c.215C=	ENSP00000459107.1:p.Thr72=
ENST00000576406.5:c.-347C=	ENSP00000461214.1:n.-347C=
ENST00000577053.1:c.215C=	ENSP00000460842.1:p.Thr72=