Canonical Allele Identifier: CA8274501

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1766925G>T , CM000679.2:g.1766925G>T	GRCh38
NC_000017.10:g.1670219G>T , CM000679.1:g.1670219G>T	GRCh37
NC_000017.9:g.1616969G>T	NCBI36
NG_028180.1:g.9961G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.15G>T MANE Select	NP_002606.3:p.Val5=
ENST00000254722.9:c.15G>T MANE Select	ENSP00000254722.4:p.Val5=
NM_001329903.1:c.15G>T	NP_001316832.1:p.Val5=
NM_001329903.2:c.15G>T	NP_001316832.1:p.Val5=
NM_001329904.1:c.-477-2927G>T	NP_001316833.1:n.-477-2927G>T
NM_001329904.2:c.-477-2927G>T	NP_001316833.1:n.-477-2927G>T
NM_002615.5:c.15G>T	NP_002606.3:p.Val5=
NM_002615.6:c.15G>T	NP_002606.3:p.Val5=
ENST00000254722.8:c.15G>T	ENSP00000254722.4:p.Val5=
ENST00000570731.5:c.15G>T	ENSP00000459869.1:p.Val5=
ENST00000571149.5:c.15G>T	ENSP00000460905.1:p.Val5=
ENST00000571360.5:c.15G>T	ENSP00000461660.1:p.Val5=
ENST00000571870.5:n.76G>T
ENST00000573770.5:c.15G>T	ENSP00000459107.1:p.Val5=
ENST00000576406.5:c.-477-2927G>T	ENSP00000461214.1:n.-477-2927G>T
ENST00000577053.1:c.15G>T	ENSP00000460842.1:p.Val5=