Canonical Allele Identifier: CA2244642442
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945884G= , CM000679.2:g.4945884G= GRCh38
NC_000017.10:g.4849179G= , CM000679.1:g.4849179G= GRCh37
NC_000017.9:g.4789924G= NCBI36
NG_012063.2:g.4794G=
NG_032945.1:g.8203C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*16C= MANE Select ENSP00000225655.5:n.*16C=
ENST00000225655.5:c.*16C= ENSP00000225655.5:n.*16C=
ENST00000574872.1:c.*16C= ENSP00000465019.1:n.*16C=
NM_005022.3:c.*16C= NP_005013.1:n.*16C=
XM_017024761.1:c.*523C= XP_016880250.1:n.*523C=
NM_001375991.1:c.*523C= NP_001362920.1:n.*523C=
NM_005022.4:c.*16C= MANE Select NP_005013.1:n.*16C=