Canonical Allele Identifier: CA263812885

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77444053_77444056dup , CM000676.2:g.77444053_77444056dup	GRCh38
NC_000014.8:g.77910396_77910399dup , CM000676.1:g.77910396_77910399dup	GRCh37
NC_000014.7:g.76980149_76980152dup	NCBI36
NG_023421.1:g.18596_18599dup
NG_023421.2:g.18596_18599dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.597+204_597+207dup MANE Select	ENSP00000452191.1:n.597+204_597+207dup
ENST00000327028.8:c.450+204_450+207dup	ENSP00000313098.5:n.450+204_450+207dup
ENST00000343765.6:c.597+204_597+207dup	ENSP00000339122.2:n.597+204_597+207dup
ENST00000448935.6:c.450+204_450+207dup	ENSP00000404815.2:n.450+204_450+207dup
ENST00000553691.5:n.487+204_487+207dup
ENST00000553888.5:c.597+204_597+207dup	ENSP00000452181.1:n.597+204_597+207dup
ENST00000555854.1:n.42+204_42+207dup
ENST00000556412.4:c.675+204_675+207dup	ENSP00000451857.1:n.675+204_675+207dup
ENST00000557658.5:c.597+204_597+207dup	ENSP00000452191.1:n.597+204_597+207dup
NM_001193314.1:c.597+204_597+207dup	NP_001180243.1:n.597+204_597+207dup
NM_001193315.1:c.597+204_597+207dup	NP_001180244.1:n.597+204_597+207dup
NM_001193316.1:c.450+204_450+207dup	NP_001180245.1:n.450+204_450+207dup
NM_001193317.1:c.597+204_597+207dup	NP_001180246.1:n.597+204_597+207dup
NM_022067.3:c.597+204_597+207dup	NP_071350.2:n.597+204_597+207dup
XM_011537066.1:c.505-893_505-890dup	XP_011535368.1:n.505-893_505-890dup
XM_011537066.2:c.505-893_505-890dup	XP_011535368.1:n.505-893_505-890dup
XM_017021580.2:c.597+204_597+207dup	XP_016877069.1:n.597+204_597+207dup
XM_017021581.2:c.597+204_597+207dup	XP_016877070.1:n.597+204_597+207dup
XM_024449688.1:c.505-893_505-890dup	XP_024305456.1:n.505-893_505-890dup
XR_001750501.2:n.719+204_719+207dup
NM_001193314.2:c.597+204_597+207dup	NP_001180243.1:n.597+204_597+207dup
NM_001193316.2:c.450+204_450+207dup	NP_001180245.1:n.450+204_450+207dup
NM_001193317.2:c.597+204_597+207dup	NP_001180246.1:n.597+204_597+207dup
NM_022067.4:c.597+204_597+207dup	NP_071350.2:n.597+204_597+207dup
NM_001193315.2:c.597+204_597+207dup MANE Select	NP_001180244.1:n.597+204_597+207dup
NM_001400324.1:c.450+204_450+207dup	NP_001387253.1:n.450+204_450+207dup
NM_001400325.1:c.450+204_450+207dup	NP_001387254.1:n.450+204_450+207dup
NM_001400326.1:c.597+204_597+207dup	NP_001387255.1:n.597+204_597+207dup
NM_001400327.1:c.564+204_564+207dup	NP_001387256.1:n.564+204_564+207dup
NM_001400330.1:c.597+204_597+207dup	NP_001387259.1:n.597+204_597+207dup
NM_001400331.1:c.597+204_597+207dup	NP_001387260.1:n.597+204_597+207dup
NM_001400332.1:c.597+204_597+207dup	NP_001387261.1:n.597+204_597+207dup
NM_001400333.1:c.505-893_505-890dup	NP_001387262.1:n.505-893_505-890dup
NM_001400334.1:c.505-893_505-890dup	NP_001387263.1:n.505-893_505-890dup
NM_001400335.1:c.597+204_597+207dup	NP_001387264.1:n.597+204_597+207dup
NM_001400336.1:c.597+204_597+207dup	NP_001387265.1:n.597+204_597+207dup
NM_001400337.1:c.358-893_358-890dup	NP_001387266.1:n.358-893_358-890dup
NM_001400338.1:c.597+204_597+207dup	NP_001387267.1:n.597+204_597+207dup
NM_001400339.1:c.597+204_597+207dup	NP_001387268.1:n.597+204_597+207dup
NR_174476.1:n.704+204_704+207dup