Canonical Allele Identifier: CA2244642829
Gene: PFN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4946057C= , CM000679.2:g.4946057C= GRCh38
NC_000017.10:g.4849352C= , CM000679.1:g.4849352C= GRCh37
NC_000017.9:g.4790097C= NCBI36
NG_012063.2:g.4967C=
NG_032945.1:g.8030G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.326-60G= MANE Select ENSP00000225655.5:n.326-60G=
ENST00000225655.5:c.326-60G= ENSP00000225655.5:n.326-60G=
ENST00000574872.1:c.218-60G= ENSP00000465019.1:n.218-60G=
NM_005022.3:c.326-60G= NP_005013.1:n.326-60G=
XM_017024761.1:c.*350G= XP_016880250.1:n.*350G=
NM_001375991.1:c.*350G= NP_001362920.1:n.*350G=
NM_005022.4:c.326-60G= MANE Select NP_005013.1:n.326-60G=
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