Canonical Allele Identifier: CA8274909

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1776754G>A , CM000679.2:g.1776754G>A	GRCh38
NC_000017.10:g.1680048G>A , CM000679.1:g.1680048G>A	GRCh37
NC_000017.9:g.1626798G>A	NCBI36
NG_028180.1:g.19790G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.997+12G>A MANE Select	NP_002606.3:n.997+12G>A
ENST00000254722.9:c.997+12G>A MANE Select	ENSP00000254722.4:n.997+12G>A
NM_001329903.1:c.997+12G>A	NP_001316832.1:n.997+12G>A
NM_001329903.2:c.997+12G>A	NP_001316832.1:n.997+12G>A
NM_001329904.1:c.436+12G>A	NP_001316833.1:n.436+12G>A
NM_001329904.2:c.436+12G>A	NP_001316833.1:n.436+12G>A
NM_001329905.1:c.436+12G>A	NP_001316834.1:n.436+12G>A
NM_001329905.2:c.436+12G>A	NP_001316834.1:n.436+12G>A
NM_002615.5:c.997+12G>A	NP_002606.3:n.997+12G>A
NM_002615.6:c.997+12G>A	NP_002606.3:n.997+12G>A
ENST00000254722.8:c.997+12G>A	ENSP00000254722.4:n.997+12G>A
ENST00000572517.1:n.293+12G>A
ENST00000573763.1:c.391+12G>A	ENSP00000461405.1:n.391+12G>A