Canonical Allele Identifier: CA383506550
Community Standard Title: NM_000552.5(VWF):c.3878T>C (p.Phe1293Ser)
Gene: VWF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6019540A>G , CM000674.2:g.6019540A>G GRCh38
NC_000012.11:g.6128706A>G , CM000674.1:g.6128706A>G GRCh37
NC_000012.10:g.5998967A>G NCBI36
NG_009072.1:g.110131T>C
NG_009072.2:g.110131T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000552.5:c.3878T>C MANE Select NP_000543.3:p.Phe1293Ser
ENST00000261405.10:c.3878T>C MANE Select ENSP00000261405.5:p.Phe1293Ser
NM_000552.3:c.3878T>C NP_000543.2:p.Phe1293Ser
NM_000552.4:c.3878T>C NP_000543.2:p.Phe1293Ser
ENST00000261405.9:c.3878T>C ENSP00000261405.5:p.Phe1293Ser
ENST00000538635.5:n.421-25606T>C
ENST00000539641.1:n.676T>C