Canonical Allele Identifier: CA397338191

Gene: PFN1

Linked Data

• MyVariant Identifiers: chr17:g.4849235C>G (hg19) ; chr17:g.4945940C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4945940C>G , CM000679.2:g.4945940C>G	GRCh38
NC_000017.10:g.4849235C>G , CM000679.1:g.4849235C>G	GRCh37
NC_000017.9:g.4789980C>G	NCBI36
NG_012063.2:g.4850C>G
NG_032945.1:g.8147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225655.6:c.383G>C MANE Select	ENSP00000225655.5:p.Cys128Ser
ENST00000225655.5:c.383G>C	ENSP00000225655.5:p.Cys128Ser
ENST00000574872.1:c.275G>C	ENSP00000465019.1:p.Cys92Ser
NM_005022.3:c.383G>C	NP_005013.1:p.Cys128Ser
XM_017024761.1:c.*467G>C	XP_016880250.1:n.*467G>C
NM_001375991.1:c.*467G>C	NP_001362920.1:n.*467G>C
NM_005022.4:c.383G>C MANE Select	NP_005013.1:p.Cys128Ser