Canonical Allele Identifier: CA2148395785

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77441050_77441051delinsCA , CM000676.2:g.77441050_77441051delinsCA	GRCh38
NC_000014.8:g.77907393_77907394delinsCA , CM000676.1:g.77907393_77907394delinsCA	GRCh37
NC_000014.7:g.76977146_76977147delinsCA	NCBI36
NG_023421.1:g.21590_21591delinsTG
NG_023421.2:g.21590_21591delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.762+15_762+16delinsTG MANE Select	ENSP00000452191.1:n.762+15_762+16delinsTG
ENST00000327028.8:c.615+15_615+16delinsTG	ENSP00000313098.5:n.615+15_615+16delinsTG
ENST00000343765.6:c.762+15_762+16delinsTG	ENSP00000339122.2:n.762+15_762+16delinsTG
ENST00000448935.6:c.615+15_615+16delinsTG	ENSP00000404815.2:n.615+15_615+16delinsTG
ENST00000553576.5:n.174+15_174+16delinsTG
ENST00000553691.5:n.732+15_732+16delinsTG
ENST00000553888.5:c.762+15_762+16delinsTG	ENSP00000452181.1:n.762+15_762+16delinsTG
ENST00000555854.1:n.207+15_207+16delinsTG
ENST00000556412.4:c.840+15_840+16delinsTG	ENSP00000451857.1:n.840+15_840+16delinsTG
ENST00000557658.5:c.762+15_762+16delinsTG	ENSP00000452191.1:n.762+15_762+16delinsTG
NM_001193314.1:c.762+15_762+16delinsTG	NP_001180243.1:n.762+15_762+16delinsTG
NM_001193315.1:c.762+15_762+16delinsTG	NP_001180244.1:n.762+15_762+16delinsTG
NM_001193316.1:c.615+15_615+16delinsTG	NP_001180245.1:n.615+15_615+16delinsTG
NM_001193317.1:c.762+15_762+16delinsTG	NP_001180246.1:n.762+15_762+16delinsTG
NM_022067.3:c.762+15_762+16delinsTG	NP_071350.2:n.762+15_762+16delinsTG
XM_011537066.1:c.669+15_669+16delinsTG	XP_011535368.1:n.669+15_669+16delinsTG
XM_011537066.2:c.669+15_669+16delinsTG	XP_011535368.1:n.669+15_669+16delinsTG
XM_017021580.2:c.762+15_762+16delinsTG	XP_016877069.1:n.762+15_762+16delinsTG
XM_017021581.2:c.762+15_762+16delinsTG	XP_016877070.1:n.762+15_762+16delinsTG
XM_024449688.1:c.669+15_669+16delinsTG	XP_024305456.1:n.669+15_669+16delinsTG
XR_001750501.2:n.884+15_884+16delinsTG
NM_001193314.2:c.762+15_762+16delinsTG	NP_001180243.1:n.762+15_762+16delinsTG
NM_001193316.2:c.615+15_615+16delinsTG	NP_001180245.1:n.615+15_615+16delinsTG
NM_001193317.2:c.762+15_762+16delinsTG	NP_001180246.1:n.762+15_762+16delinsTG
NM_022067.4:c.762+15_762+16delinsTG	NP_071350.2:n.762+15_762+16delinsTG
NM_001193315.2:c.762+15_762+16delinsTG MANE Select	NP_001180244.1:n.762+15_762+16delinsTG
NM_001400324.1:c.615+15_615+16delinsTG	NP_001387253.1:n.615+15_615+16delinsTG
NM_001400325.1:c.615+15_615+16delinsTG	NP_001387254.1:n.615+15_615+16delinsTG
NM_001400326.1:c.762+15_762+16delinsTG	NP_001387255.1:n.762+15_762+16delinsTG
NM_001400327.1:c.729+15_729+16delinsTG	NP_001387256.1:n.729+15_729+16delinsTG
NM_001400330.1:c.762+15_762+16delinsTG	NP_001387259.1:n.762+15_762+16delinsTG
NM_001400331.1:c.762+15_762+16delinsTG	NP_001387260.1:n.762+15_762+16delinsTG
NM_001400332.1:c.762+15_762+16delinsTG	NP_001387261.1:n.762+15_762+16delinsTG
NM_001400333.1:c.669+15_669+16delinsTG	NP_001387262.1:n.669+15_669+16delinsTG
NM_001400334.1:c.669+15_669+16delinsTG	NP_001387263.1:n.669+15_669+16delinsTG
NM_001400335.1:c.762+15_762+16delinsTG	NP_001387264.1:n.762+15_762+16delinsTG
NM_001400336.1:c.762+15_762+16delinsTG	NP_001387265.1:n.762+15_762+16delinsTG
NM_001400337.1:c.522+15_522+16delinsTG	NP_001387266.1:n.522+15_522+16delinsTG
NM_001400338.1:c.734+1509_734+1510delinsTG	NP_001387267.1:n.734+1509_734+1510delinsTG
NM_001400339.1:c.762+15_762+16delinsTG	NP_001387268.1:n.762+15_762+16delinsTG
NR_174476.1:n.869+15_869+16delinsTG