Canonical Allele Identifier: CA2244642542
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945957A= , CM000679.2:g.4945957A= GRCh38
NC_000017.10:g.4849252A= , CM000679.1:g.4849252A= GRCh37
NC_000017.9:g.4789997A= NCBI36
NG_012063.2:g.4867A=
NG_032945.1:g.8130T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.366T= MANE Select ENSP00000225655.5:p.Gly122=
ENST00000225655.5:c.366T= ENSP00000225655.5:p.Gly122=
ENST00000574872.1:c.258T= ENSP00000465019.1:p.Gly86=
NM_005022.3:c.366T= NP_005013.1:p.Gly122=
XM_017024761.1:c.*450T= XP_016880250.1:n.*450T=
NM_001375991.1:c.*450T= NP_001362920.1:n.*450T=
NM_005022.4:c.366T= MANE Select NP_005013.1:p.Gly122=