Canonical Allele Identifier: CA2244642584
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945972T= , CM000679.2:g.4945972T= GRCh38
NC_000017.10:g.4849267T= , CM000679.1:g.4849267T= GRCh37
NC_000017.9:g.4790012T= NCBI36
NG_012063.2:g.4882T=
NG_032945.1:g.8115A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.351A= MANE Select ENSP00000225655.5:p.Glu117=
ENST00000225655.5:c.351A= ENSP00000225655.5:p.Glu117=
ENST00000574872.1:c.243A= ENSP00000465019.1:p.Glu81=
NM_005022.3:c.351A= NP_005013.1:p.Glu117=
XM_017024761.1:c.*435A= XP_016880250.1:n.*435A=
NM_001375991.1:c.*435A= NP_001362920.1:n.*435A=
NM_005022.4:c.351A= MANE Select NP_005013.1:p.Glu117=