Canonical Allele Identifier: CA2148395826

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77441146_77441150delinsTATAA , CM000676.2:g.77441146_77441150delinsTATAA	GRCh38
NC_000014.8:g.77907489_77907493delinsTATAA , CM000676.1:g.77907489_77907493delinsTATAA	GRCh37
NC_000014.7:g.76977242_76977246delinsTATAA	NCBI36
NG_023421.1:g.21491_21495delinsTTATA
NG_023421.2:g.21491_21495delinsTTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.735-57_735-53delinsTTATA MANE Select	ENSP00000452191.1:n.735-57_735-53delinsTTATA
ENST00000327028.8:c.588-57_588-53delinsTTATA	ENSP00000313098.5:n.588-57_588-53delinsTTATA
ENST00000343765.6:c.735-57_735-53delinsTTATA	ENSP00000339122.2:n.735-57_735-53delinsTTATA
ENST00000448935.6:c.588-57_588-53delinsTTATA	ENSP00000404815.2:n.588-57_588-53delinsTTATA
ENST00000553576.5:n.147-57_147-53delinsTTATA
ENST00000553691.5:n.648_652delinsTTATA
ENST00000553888.5:c.735-57_735-53delinsTTATA	ENSP00000452181.1:n.735-57_735-53delinsTTATA
ENST00000555854.1:n.180-57_180-53delinsTTATA
ENST00000556412.4:c.813-57_813-53delinsTTATA	ENSP00000451857.1:n.813-57_813-53delinsTTATA
ENST00000557658.5:c.735-57_735-53delinsTTATA	ENSP00000452191.1:n.735-57_735-53delinsTTATA
NM_001193314.1:c.735-57_735-53delinsTTATA	NP_001180243.1:n.735-57_735-53delinsTTATA
NM_001193315.1:c.735-57_735-53delinsTTATA	NP_001180244.1:n.735-57_735-53delinsTTATA
NM_001193316.1:c.588-57_588-53delinsTTATA	NP_001180245.1:n.588-57_588-53delinsTTATA
NM_001193317.1:c.735-57_735-53delinsTTATA	NP_001180246.1:n.735-57_735-53delinsTTATA
NM_022067.3:c.735-57_735-53delinsTTATA	NP_071350.2:n.735-57_735-53delinsTTATA
XM_011537066.1:c.642-57_642-53delinsTTATA	XP_011535368.1:n.642-57_642-53delinsTTATA
XM_011537066.2:c.642-57_642-53delinsTTATA	XP_011535368.1:n.642-57_642-53delinsTTATA
XM_017021580.2:c.735-57_735-53delinsTTATA	XP_016877069.1:n.735-57_735-53delinsTTATA
XM_017021581.2:c.735-57_735-53delinsTTATA	XP_016877070.1:n.735-57_735-53delinsTTATA
XM_024449688.1:c.642-57_642-53delinsTTATA	XP_024305456.1:n.642-57_642-53delinsTTATA
XR_001750501.2:n.857-57_857-53delinsTTATA
NM_001193314.2:c.735-57_735-53delinsTTATA	NP_001180243.1:n.735-57_735-53delinsTTATA
NM_001193316.2:c.588-57_588-53delinsTTATA	NP_001180245.1:n.588-57_588-53delinsTTATA
NM_001193317.2:c.735-57_735-53delinsTTATA	NP_001180246.1:n.735-57_735-53delinsTTATA
NM_022067.4:c.735-57_735-53delinsTTATA	NP_071350.2:n.735-57_735-53delinsTTATA
NM_001193315.2:c.735-57_735-53delinsTTATA MANE Select	NP_001180244.1:n.735-57_735-53delinsTTATA
NM_001400324.1:c.588-57_588-53delinsTTATA	NP_001387253.1:n.588-57_588-53delinsTTATA
NM_001400325.1:c.588-57_588-53delinsTTATA	NP_001387254.1:n.588-57_588-53delinsTTATA
NM_001400326.1:c.735-57_735-53delinsTTATA	NP_001387255.1:n.735-57_735-53delinsTTATA
NM_001400327.1:c.702-57_702-53delinsTTATA	NP_001387256.1:n.702-57_702-53delinsTTATA
NM_001400330.1:c.735-57_735-53delinsTTATA	NP_001387259.1:n.735-57_735-53delinsTTATA
NM_001400331.1:c.735-57_735-53delinsTTATA	NP_001387260.1:n.735-57_735-53delinsTTATA
NM_001400332.1:c.735-57_735-53delinsTTATA	NP_001387261.1:n.735-57_735-53delinsTTATA
NM_001400333.1:c.642-57_642-53delinsTTATA	NP_001387262.1:n.642-57_642-53delinsTTATA
NM_001400334.1:c.642-57_642-53delinsTTATA	NP_001387263.1:n.642-57_642-53delinsTTATA
NM_001400335.1:c.735-57_735-53delinsTTATA	NP_001387264.1:n.735-57_735-53delinsTTATA
NM_001400336.1:c.735-57_735-53delinsTTATA	NP_001387265.1:n.735-57_735-53delinsTTATA
NM_001400337.1:c.495-57_495-53delinsTTATA	NP_001387266.1:n.495-57_495-53delinsTTATA
NM_001400338.1:c.734+1410_734+1414delinsTTATA	NP_001387267.1:n.734+1410_734+1414delinsTTATA
NM_001400339.1:c.735-57_735-53delinsTTATA	NP_001387268.1:n.735-57_735-53delinsTTATA
NR_174476.1:n.842-57_842-53delinsTTATA