Canonical Allele Identifier: CA624473855
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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