Canonical Allele Identifier: CA2243026389

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772177T= , CM000679.2:g.1772177T=	GRCh38
NC_000017.10:g.1675471T= , CM000679.1:g.1675471T=	GRCh37
NC_000017.9:g.1622221T=	NCBI36
NG_028180.1:g.15213T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.643+102T= MANE Select	ENSP00000254722.4:n.643+102T=
ENST00000254722.8:c.643+102T=	ENSP00000254722.4:n.643+102T=
ENST00000572048.1:c.82+102T=	ENSP00000458484.1:n.82+102T=
ENST00000573763.1:c.42+102T=	ENSP00000461405.1:n.42+102T=
ENST00000576406.5:c.82+102T=	ENSP00000461214.1:n.82+102T=
NM_002615.5:c.643+102T=	NP_002606.3:n.643+102T=
NM_001329903.1:c.643+102T=	NP_001316832.1:n.643+102T=
NM_001329904.1:c.82+102T=	NP_001316833.1:n.82+102T=
NM_001329905.1:c.82+102T=	NP_001316834.1:n.82+102T=
NM_002615.6:c.643+102T=	NP_002606.3:n.643+102T=
NM_002615.7:c.643+102T= MANE Select	NP_002606.3:n.643+102T=
NM_001329903.2:c.643+102T=	NP_001316832.1:n.643+102T=
NM_001329904.2:c.82+102T=	NP_001316833.1:n.82+102T=
NM_001329905.2:c.82+102T=	NP_001316834.1:n.82+102T=