Canonical Allele Identifier: CA2148397011

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77443966_77443976delinsAGGAGGTCGAG , CM000676.2:g.77443966_77443976delinsAGGAGGTCGAG	GRCh38
NC_000014.8:g.77910309_77910319delinsAGGAGGTCGAG , CM000676.1:g.77910309_77910319delinsAGGAGGTCGAG	GRCh37
NC_000014.7:g.76980062_76980072delinsAGGAGGTCGAG	NCBI36
NG_023421.1:g.18665_18675delinsCTCGACCTCCT
NG_023421.2:g.18665_18675delinsCTCGACCTCCT

Transcript Alleles

HGVS	Amino-acid Change
NM_001193315.2:c.597+273_597+283delinsCTCGACCTCCT MANE Select	NP_001180244.1:n.597+273_597+283delinsCTCGACCTCCT
ENST00000557658.6:c.597+273_597+283delinsCTCGACCTCCT MANE Select	ENSP00000452191.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001193314.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001180243.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001193314.2:c.597+273_597+283delinsCTCGACCTCCT	NP_001180243.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001193315.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001180244.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001193316.1:c.450+273_450+283delinsCTCGACCTCCT	NP_001180245.1:n.450+273_450+283delinsCTCGACCTCCT
NM_001193316.2:c.450+273_450+283delinsCTCGACCTCCT	NP_001180245.1:n.450+273_450+283delinsCTCGACCTCCT
NM_001193317.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001180246.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001193317.2:c.597+273_597+283delinsCTCGACCTCCT	NP_001180246.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400324.1:c.450+273_450+283delinsCTCGACCTCCT	NP_001387253.1:n.450+273_450+283delinsCTCGACCTCCT
NM_001400325.1:c.450+273_450+283delinsCTCGACCTCCT	NP_001387254.1:n.450+273_450+283delinsCTCGACCTCCT
NM_001400326.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387255.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400327.1:c.564+273_564+283delinsCTCGACCTCCT	NP_001387256.1:n.564+273_564+283delinsCTCGACCTCCT
NM_001400330.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387259.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400331.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387260.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400332.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387261.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400333.1:c.505-824_505-814delinsCTCGACCTCCT	NP_001387262.1:n.505-824_505-814delinsCTCGACCTCCT
NM_001400334.1:c.505-824_505-814delinsCTCGACCTCCT	NP_001387263.1:n.505-824_505-814delinsCTCGACCTCCT
NM_001400335.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387264.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400336.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387265.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400337.1:c.358-824_358-814delinsCTCGACCTCCT	NP_001387266.1:n.358-824_358-814delinsCTCGACCTCCT
NM_001400338.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387267.1:n.597+273_597+283delinsCTCGACCTCCT
NM_001400339.1:c.597+273_597+283delinsCTCGACCTCCT	NP_001387268.1:n.597+273_597+283delinsCTCGACCTCCT
NM_022067.3:c.597+273_597+283delinsCTCGACCTCCT	NP_071350.2:n.597+273_597+283delinsCTCGACCTCCT
NM_022067.4:c.597+273_597+283delinsCTCGACCTCCT	NP_071350.2:n.597+273_597+283delinsCTCGACCTCCT
NR_174476.1:n.704+273_704+283delinsCTCGACCTCCT
ENST00000327028.8:c.450+273_450+283delinsCTCGACCTCCT	ENSP00000313098.5:n.450+273_450+283delinsCTCGACCTCCT
ENST00000343765.6:c.597+273_597+283delinsCTCGACCTCCT	ENSP00000339122.2:n.597+273_597+283delinsCTCGACCTCCT
ENST00000448935.6:c.450+273_450+283delinsCTCGACCTCCT	ENSP00000404815.2:n.450+273_450+283delinsCTCGACCTCCT
ENST00000553691.5:n.487+273_487+283delinsCTCGACCTCCT
ENST00000553888.5:c.597+273_597+283delinsCTCGACCTCCT	ENSP00000452181.1:n.597+273_597+283delinsCTCGACCTCCT
ENST00000555854.1:n.42+273_42+283delinsCTCGACCTCCT
ENST00000556412.4:c.675+273_675+283delinsCTCGACCTCCT	ENSP00000451857.1:n.675+273_675+283delinsCTCGACCTCCT
ENST00000557658.5:c.597+273_597+283delinsCTCGACCTCCT	ENSP00000452191.1:n.597+273_597+283delinsCTCGACCTCCT
XM_011537066.1:c.505-824_505-814delinsCTCGACCTCCT	XP_011535368.1:n.505-824_505-814delinsCTCGACCTCCT
XM_011537066.2:c.505-824_505-814delinsCTCGACCTCCT	XP_011535368.1:n.505-824_505-814delinsCTCGACCTCCT
XM_017021580.2:c.597+273_597+283delinsCTCGACCTCCT	XP_016877069.1:n.597+273_597+283delinsCTCGACCTCCT
XM_017021581.2:c.597+273_597+283delinsCTCGACCTCCT	XP_016877070.1:n.597+273_597+283delinsCTCGACCTCCT
XM_024449688.1:c.505-824_505-814delinsCTCGACCTCCT	XP_024305456.1:n.505-824_505-814delinsCTCGACCTCCT
XR_001750501.2:n.719+273_719+283delinsCTCGACCTCCT