Canonical Allele Identifier: CA2244642318
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945847A= , CM000679.2:g.4945847A= GRCh38
NC_000017.10:g.4849142A= , CM000679.1:g.4849142A= GRCh37
NC_000017.9:g.4789887A= NCBI36
NG_012063.2:g.4757A=
NG_032945.1:g.8240T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*53T= MANE Select ENSP00000225655.5:n.*53T=
ENST00000225655.5:c.*53T= ENSP00000225655.5:n.*53T=
ENST00000574872.1:c.*53T= ENSP00000465019.1:n.*53T=
NM_005022.3:c.*53T= NP_005013.1:n.*53T=
XM_017024761.1:c.*560T= XP_016880250.1:n.*560T=
NM_001375991.1:c.*560T= NP_001362920.1:n.*560T=
NM_005022.4:c.*53T= MANE Select NP_005013.1:n.*53T=