Canonical Allele Identifier: CA2244642283
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945832T= , CM000679.2:g.4945832T= GRCh38
NC_000017.10:g.4849127T= , CM000679.1:g.4849127T= GRCh37
NC_000017.9:g.4789872T= NCBI36
NG_012063.2:g.4742T=
NG_032945.1:g.8255A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*68A= MANE Select ENSP00000225655.5:n.*68A=
ENST00000225655.5:c.*68A= ENSP00000225655.5:n.*68A=
ENST00000574872.1:c.*68A= ENSP00000465019.1:n.*68A=
NM_005022.3:c.*68A= NP_005013.1:n.*68A=
XM_017024761.1:c.*575A= XP_016880250.1:n.*575A=
NM_001375991.1:c.*575A= NP_001362920.1:n.*575A=
NM_005022.4:c.*68A= MANE Select NP_005013.1:n.*68A=