Canonical Allele Identifier: CA397337961

Gene: PFN1

Linked Data

• MyVariant Identifiers: chr17:g.4849195T>G (hg19) ; chr17:g.4945900T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4945900T>G , CM000679.2:g.4945900T>G	GRCh38
NC_000017.10:g.4849195T>G , CM000679.1:g.4849195T>G	GRCh37
NC_000017.9:g.4789940T>G	NCBI36
NG_012063.2:g.4810T>G
NG_032945.1:g.8187A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225655.6:c.423A>C MANE Select	ENSP00000225655.5:p.Ter141Cys
ENST00000225655.5:c.423A>C	ENSP00000225655.5:p.Ter141Cys
ENST00000574872.1:c.315A>C	ENSP00000465019.1:p.Ter105Cys
NM_005022.3:c.423A>C	NP_005013.1:p.Ter141Cys
XM_017024761.1:c.*507A>C	XP_016880250.1:n.*507A>C
NM_001375991.1:c.*507A>C	NP_001362920.1:n.*507A>C
NM_005022.4:c.423A>C MANE Select	NP_005013.1:p.Ter141Cys