Canonical Allele Identifier: CA2244642358
Gene: PFN1 HGNC NCBI

Linked Data

dbSNP Id: rs1971374058
gnomAD v4: 17-4945858-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4945858G>A , CM000679.2:g.4945858G>A GRCh38
NC_000017.10:g.4849153G>A , CM000679.1:g.4849153G>A GRCh37
NC_000017.9:g.4789898G>A NCBI36
NG_012063.2:g.4768G>A
NG_032945.1:g.8229C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225655.6:c.*42C>T MANE Select ENSP00000225655.5:n.*42C>T
ENST00000225655.5:c.*42C>T ENSP00000225655.5:n.*42C>T
ENST00000574872.1:c.*42C>T ENSP00000465019.1:n.*42C>T
NM_005022.3:c.*42C>T NP_005013.1:n.*42C>T
XM_017024761.1:c.*549C>T XP_016880250.1:n.*549C>T
NM_001375991.1:c.*549C>T NP_001362920.1:n.*549C>T
NM_005022.4:c.*42C>T MANE Select NP_005013.1:n.*42C>T