Canonical Allele Identifier: CA397005406
Community Standard Title: NM_001451.3(FOXF1):c.179C>T (p.Ala60Val)
Gene: FOXF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510748C>T , CM000678.2:g.86510748C>T GRCh38
NC_000016.9:g.86544354C>T , CM000678.1:g.86544354C>T GRCh37
NC_000016.8:g.85101855C>T NCBI36
NG_016273.1:g.5222C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001451.3:c.179C>T MANE Select NP_001442.2:p.Ala60Val
ENST00000262426.6:c.179C>T MANE Select ENSP00000262426.4:p.Ala60Val
NM_001451.2:c.179C>T NP_001442.2:p.Ala60Val
ENST00000262426.5:c.179C>T ENSP00000262426.4:p.Ala60Val
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