Canonical Allele Identifier: CA2244642361
Gene: PFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945859C= , CM000679.2:g.4945859C= GRCh38
NC_000017.10:g.4849154C= , CM000679.1:g.4849154C= GRCh37
NC_000017.9:g.4789899C= NCBI36
NG_012063.2:g.4769C=
NG_032945.1:g.8228G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*41G= MANE Select ENSP00000225655.5:n.*41G=
ENST00000225655.5:c.*41G= ENSP00000225655.5:n.*41G=
ENST00000574872.1:c.*41G= ENSP00000465019.1:n.*41G=
NM_005022.3:c.*41G= NP_005013.1:n.*41G=
XM_017024761.1:c.*548G= XP_016880250.1:n.*548G=
NM_001375991.1:c.*548G= NP_001362920.1:n.*548G=
NM_005022.4:c.*41G= MANE Select NP_005013.1:n.*41G=