Canonical Allele Identifier: CA3223305019
Community Standard Title: NM_002615.7(SERPINF1):c.653T= (p.Val218=)
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1775067T= , CM000679.2:g.1775067T= GRCh38
NC_000017.10:g.1678361T= , CM000679.1:g.1678361T= GRCh37
NC_000017.9:g.1625111T= NCBI36
NG_028180.1:g.18103T=

Transcript Alleles

HGVS Amino-acid Change
NM_002615.7:c.653T= MANE Select NP_002606.3:p.Val218=
ENST00000254722.9:c.653T= MANE Select ENSP00000254722.4:p.Val218=
NM_001329903.1:c.653T= NP_001316832.1:p.Val218=
NM_001329903.2:c.653T= NP_001316832.1:p.Val218=
NM_001329904.1:c.92T= NP_001316833.1:p.Val31=
NM_001329904.2:c.92T= NP_001316833.1:p.Val31=
NM_001329905.1:c.92T= NP_001316834.1:p.Val31=
NM_001329905.2:c.92T= NP_001316834.1:p.Val31=
NM_002615.5:c.653T= NP_002606.3:p.Val218=
NM_002615.6:c.653T= NP_002606.3:p.Val218=
ENST00000254722.8:c.653T= ENSP00000254722.4:p.Val218=
ENST00000572048.1:c.92T= ENSP00000458484.1:p.Val31=
ENST00000573763.1:c.47T= ENSP00000461405.1:p.Val16=
ENST00000576406.5:c.92T= ENSP00000461214.1:p.Val31=