Canonical Allele Identifier: CA390697156
Gene: VIPAS39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77435350A>G , CM000676.2:g.77435350A>G GRCh38
NC_000014.8:g.77901693A>G , CM000676.1:g.77901693A>G GRCh37
NC_000014.7:g.76971446A>G NCBI36
NG_023421.1:g.27291T>C
NG_023421.2:g.27291T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000557658.6:c.956T>C MANE Select ENSP00000452191.1:p.Phe319Ser
ENST00000327028.8:c.809T>C ENSP00000313098.5:p.Phe270Ser
ENST00000343765.6:c.956T>C ENSP00000339122.2:p.Phe319Ser
ENST00000448935.6:c.809T>C ENSP00000404815.2:p.Phe270Ser
ENST00000553576.5:n.368T>C
ENST00000553888.5:c.956T>C ENSP00000452181.1:p.Phe319Ser
ENST00000556412.4:c.1034T>C ENSP00000451857.1:p.Phe345Ser
ENST00000557658.5:c.956T>C ENSP00000452191.1:p.Phe319Ser
NM_001193314.1:c.956T>C NP_001180243.1:p.Phe319Ser
NM_001193315.1:c.956T>C NP_001180244.1:p.Phe319Ser
NM_001193316.1:c.809T>C NP_001180245.1:p.Phe270Ser
NM_001193317.1:c.956T>C NP_001180246.1:p.Phe319Ser
NM_022067.3:c.956T>C NP_071350.2:p.Phe319Ser
XM_011537066.1:c.863T>C XP_011535368.1:p.Phe288Ser
XM_011537066.2:c.863T>C XP_011535368.1:p.Phe288Ser
XM_017021580.2:c.956T>C XP_016877069.1:p.Phe319Ser
XM_017021581.2:c.956T>C XP_016877070.1:p.Phe319Ser
XM_024449688.1:c.863T>C XP_024305456.1:p.Phe288Ser
XR_001750501.2:n.1078T>C
NM_001193314.2:c.956T>C NP_001180243.1:p.Phe319Ser
NM_001193316.2:c.809T>C NP_001180245.1:p.Phe270Ser
NM_001193317.2:c.956T>C NP_001180246.1:p.Phe319Ser
NM_022067.4:c.956T>C NP_071350.2:p.Phe319Ser
NM_001193315.2:c.956T>C MANE Select NP_001180244.1:p.Phe319Ser
NM_001400324.1:c.809T>C NP_001387253.1:p.Phe270Ser
NM_001400325.1:c.809T>C NP_001387254.1:p.Phe270Ser
NM_001400326.1:c.956T>C NP_001387255.1:p.Phe319Ser
NM_001400327.1:c.923T>C NP_001387256.1:p.Phe308Ser
NM_001400330.1:c.956T>C NP_001387259.1:p.Phe319Ser
NM_001400331.1:c.956T>C NP_001387260.1:p.Phe319Ser
NM_001400332.1:c.956T>C NP_001387261.1:p.Phe319Ser
NM_001400333.1:c.863T>C NP_001387262.1:p.Phe288Ser
NM_001400334.1:c.863T>C NP_001387263.1:p.Phe288Ser
NM_001400335.1:c.956T>C NP_001387264.1:p.Phe319Ser
NM_001400336.1:c.912+494T>C NP_001387265.1:n.912+494T>C
NM_001400337.1:c.716T>C NP_001387266.1:p.Phe239Ser
NM_001400338.1:c.854T>C NP_001387267.1:p.Phe285Ser
NM_001400339.1:c.763-1047T>C NP_001387268.1:n.763-1047T>C
NR_174476.1:n.1063T>C