Canonical Allele Identifier: CA2243026251
Gene: SERPINF1 HGNC NCBI

Linked Data

dbSNP Id: rs1907781996

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1772100del , CM000679.2:g.1772100del GRCh38
NC_000017.10:g.1675394del , CM000679.1:g.1675394del GRCh37
NC_000017.9:g.1622144del NCBI36
NG_028180.1:g.15136del

Transcript Alleles

HGVS Amino-acid Change
ENST00000254722.9:c.643+25del MANE Select ENSP00000254722.4:n.643+25del
ENST00000254722.8:c.643+25del ENSP00000254722.4:n.643+25del
ENST00000572048.1:c.82+25del ENSP00000458484.1:n.82+25del
ENST00000573763.1:c.42+25del ENSP00000461405.1:n.42+25del
ENST00000576406.5:c.82+25del ENSP00000461214.1:n.82+25del
NM_002615.5:c.643+25del NP_002606.3:n.643+25del
NM_001329903.1:c.643+25del NP_001316832.1:n.643+25del
NM_001329904.1:c.82+25del NP_001316833.1:n.82+25del
NM_001329905.1:c.82+25del NP_001316834.1:n.82+25del
NM_002615.6:c.643+25del NP_002606.3:n.643+25del
NM_002615.7:c.643+25del MANE Select NP_002606.3:n.643+25del
NM_001329903.2:c.643+25del NP_001316832.1:n.643+25del
NM_001329904.2:c.82+25del NP_001316833.1:n.82+25del
NM_001329905.2:c.82+25del NP_001316834.1:n.82+25del