Canonical Allele Identifier: CA2244642471
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945896G= , CM000679.2:g.4945896G= GRCh38
NC_000017.10:g.4849191G= , CM000679.1:g.4849191G= GRCh37
NC_000017.9:g.4789936G= NCBI36
NG_012063.2:g.4806G=
NG_032945.1:g.8191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*4C= MANE Select ENSP00000225655.5:n.*4C=
ENST00000225655.5:c.*4C= ENSP00000225655.5:n.*4C=
ENST00000574872.1:c.*4C= ENSP00000465019.1:n.*4C=
NM_005022.3:c.*4C= NP_005013.1:n.*4C=
XM_017024761.1:c.*511C= XP_016880250.1:n.*511C=
NM_001375991.1:c.*511C= NP_001362920.1:n.*511C=
NM_005022.4:c.*4C= MANE Select NP_005013.1:n.*4C=