Canonical Allele Identifier: CA2244642408
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945875G= , CM000679.2:g.4945875G= GRCh38
NC_000017.10:g.4849170G= , CM000679.1:g.4849170G= GRCh37
NC_000017.9:g.4789915G= NCBI36
NG_012063.2:g.4785G=
NG_032945.1:g.8212C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*25C= MANE Select ENSP00000225655.5:n.*25C=
ENST00000225655.5:c.*25C= ENSP00000225655.5:n.*25C=
ENST00000574872.1:c.*25C= ENSP00000465019.1:n.*25C=
NM_005022.3:c.*25C= NP_005013.1:n.*25C=
XM_017024761.1:c.*532C= XP_016880250.1:n.*532C=
NM_001375991.1:c.*532C= NP_001362920.1:n.*532C=
NM_005022.4:c.*25C= MANE Select NP_005013.1:n.*25C=