Canonical Allele Identifier: CA7287955
Community Standard Title: NM_001193315.2(VIPAS39):c.808C>T (p.Arg270Ter)
Gene: VIPAS39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77437836G>A , CM000676.2:g.77437836G>A GRCh38
NC_000014.8:g.77904179G>A , CM000676.1:g.77904179G>A GRCh37
NC_000014.7:g.76973932G>A NCBI36
NG_023421.1:g.24805C>T
NG_023421.2:g.24805C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001193315.2:c.808C>T MANE Select NP_001180244.1:p.Arg270Ter
ENST00000557658.6:c.808C>T MANE Select ENSP00000452191.1:p.Arg270Ter
NM_001193314.1:c.808C>T NP_001180243.1:p.Arg270Ter
NM_001193314.2:c.808C>T NP_001180243.1:p.Arg270Ter
NM_001193315.1:c.808C>T NP_001180244.1:p.Arg270Ter
NM_001193316.1:c.661C>T NP_001180245.1:p.Arg221Ter
NM_001193316.2:c.661C>T NP_001180245.1:p.Arg221Ter
NM_001193317.1:c.808C>T NP_001180246.1:p.Arg270Ter
NM_001193317.2:c.808C>T NP_001180246.1:p.Arg270Ter
NM_001400324.1:c.661C>T NP_001387253.1:p.Arg221Ter
NM_001400325.1:c.661C>T NP_001387254.1:p.Arg221Ter
NM_001400326.1:c.808C>T NP_001387255.1:p.Arg270Ter
NM_001400327.1:c.775C>T NP_001387256.1:p.Arg259Ter
NM_001400330.1:c.808C>T NP_001387259.1:p.Arg270Ter
NM_001400331.1:c.808C>T NP_001387260.1:p.Arg270Ter
NM_001400332.1:c.808C>T NP_001387261.1:p.Arg270Ter
NM_001400333.1:c.715C>T NP_001387262.1:p.Arg239Ter
NM_001400334.1:c.715C>T NP_001387263.1:p.Arg239Ter
NM_001400335.1:c.808C>T NP_001387264.1:p.Arg270Ter
NM_001400336.1:c.808C>T NP_001387265.1:p.Arg270Ter
NM_001400337.1:c.568C>T NP_001387266.1:p.Arg190Ter
NM_001400338.1:c.735-1917C>T NP_001387267.1:n.735-1917C>T
NM_001400339.1:c.762+3230C>T NP_001387268.1:n.762+3230C>T
NM_022067.3:c.808C>T NP_071350.2:p.Arg270Ter
NM_022067.4:c.808C>T NP_071350.2:p.Arg270Ter
NR_174476.1:n.915C>T
ENST00000327028.8:c.661C>T ENSP00000313098.5:p.Arg221Ter
ENST00000343765.6:c.808C>T ENSP00000339122.2:p.Arg270Ter
ENST00000448935.6:c.661C>T ENSP00000404815.2:p.Arg221Ter
ENST00000553576.5:n.220C>T
ENST00000553691.5:n.778C>T
ENST00000553888.5:c.808C>T ENSP00000452181.1:p.Arg270Ter
ENST00000556412.4:c.886C>T ENSP00000451857.1:p.Arg296Ter
ENST00000557658.5:c.808C>T ENSP00000452191.1:p.Arg270Ter
XM_011537066.1:c.715C>T XP_011535368.1:p.Arg239Ter
XM_011537066.2:c.715C>T XP_011535368.1:p.Arg239Ter
XM_017021580.2:c.808C>T XP_016877069.1:p.Arg270Ter
XM_017021581.2:c.808C>T XP_016877070.1:p.Arg270Ter
XM_024449688.1:c.715C>T XP_024305456.1:p.Arg239Ter
XR_001750501.2:n.930C>T