Canonical Allele Identifier: CA2243021740

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1769810G= , CM000679.2:g.1769810G=	GRCh38
NC_000017.10:g.1673104G= , CM000679.1:g.1673104G=	GRCh37
NC_000017.9:g.1619854G=	NCBI36
NG_028180.1:g.12846G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.85-42G= MANE Select	NP_002606.3:n.85-42G=
ENST00000254722.9:c.85-42G= MANE Select	ENSP00000254722.4:n.85-42G=
NM_001329903.1:c.85-42G=	NP_001316832.1:n.85-42G=
NM_001329903.2:c.85-42G=	NP_001316832.1:n.85-42G=
NM_001329904.1:c.-477-42G=	NP_001316833.1:n.-477-42G=
NM_001329904.2:c.-477-42G=	NP_001316833.1:n.-477-42G=
NM_002615.5:c.85-42G=	NP_002606.3:n.85-42G=
NM_002615.6:c.85-42G=	NP_002606.3:n.85-42G=
ENST00000254722.8:c.85-42G=	ENSP00000254722.4:n.85-42G=
ENST00000570731.5:c.85-42G=	ENSP00000459869.1:n.85-42G=
ENST00000571149.5:c.85-42G=	ENSP00000460905.1:n.85-42G=
ENST00000571360.5:c.85-81G=	ENSP00000461660.1:n.85-81G=
ENST00000571870.5:n.284G=
ENST00000573770.5:c.85-42G=	ENSP00000459107.1:n.85-42G=
ENST00000576406.5:c.-477-42G=	ENSP00000461214.1:n.-477-42G=
ENST00000577053.1:c.85-42G=	ENSP00000460842.1:n.85-42G=