Canonical Allele Identifier: CA7287796

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77429751G>A , CM000676.2:g.77429751G>A	GRCh38
NC_000014.8:g.77896094G>A , CM000676.1:g.77896094G>A	GRCh37
NC_000014.7:g.76965847G>A	NCBI36
NG_023421.1:g.32890C>T
NG_023421.2:g.32890C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557658.6:c.1196C>T MANE Select	ENSP00000452191.1:p.Thr399Ile
ENST00000327028.8:c.1049C>T	ENSP00000313098.5:p.Thr350Ile
ENST00000343765.6:c.1196C>T	ENSP00000339122.2:p.Thr399Ile
ENST00000448935.6:c.1049C>T	ENSP00000404815.2:p.Thr350Ile
ENST00000553888.5:c.1196C>T	ENSP00000452181.1:p.Thr399Ile
ENST00000556412.4:c.1274C>T	ENSP00000451857.1:p.Thr425Ile
ENST00000557658.5:c.1196C>T	ENSP00000452191.1:p.Thr399Ile
NM_001193314.1:c.1196C>T	NP_001180243.1:p.Thr399Ile
NM_001193315.1:c.1196C>T	NP_001180244.1:p.Thr399Ile
NM_001193316.1:c.1049C>T	NP_001180245.1:p.Thr350Ile
NM_001193317.1:c.1196C>T	NP_001180246.1:p.Thr399Ile
NM_022067.3:c.1196C>T	NP_071350.2:p.Thr399Ile
XM_011537066.1:c.1103C>T	XP_011535368.1:p.Thr368Ile
XM_011537066.2:c.1103C>T	XP_011535368.1:p.Thr368Ile
XM_024449688.1:c.1103C>T	XP_024305456.1:p.Thr368Ile
XR_001750501.2:n.1411C>T
NM_001193314.2:c.1196C>T	NP_001180243.1:p.Thr399Ile
NM_001193316.2:c.1049C>T	NP_001180245.1:p.Thr350Ile
NM_001193317.2:c.1196C>T	NP_001180246.1:p.Thr399Ile
NM_022067.4:c.1196C>T	NP_071350.2:p.Thr399Ile
NM_001193315.2:c.1196C>T MANE Select	NP_001180244.1:p.Thr399Ile
NM_001400324.1:c.1049C>T	NP_001387253.1:p.Thr350Ile
NM_001400325.1:c.1049C>T	NP_001387254.1:p.Thr350Ile
NM_001400326.1:c.1196C>T	NP_001387255.1:p.Thr399Ile
NM_001400327.1:c.1163C>T	NP_001387256.1:p.Thr388Ile
NM_001400330.1:c.1180-656C>T	NP_001387259.1:n.1180-656C>T
NM_001400331.1:c.1180-656C>T	NP_001387260.1:n.1180-656C>T
NM_001400332.1:c.1180-656C>T	NP_001387261.1:n.1180-656C>T
NM_001400333.1:c.1103C>T	NP_001387262.1:p.Thr368Ile
NM_001400334.1:c.1103C>T	NP_001387263.1:p.Thr368Ile
NM_001400335.1:c.1196C>T	NP_001387264.1:p.Thr399Ile
NM_001400336.1:c.1061C>T	NP_001387265.1:p.Thr354Ile
NM_001400337.1:c.956C>T	NP_001387266.1:p.Thr319Ile
NM_001400338.1:c.988-656C>T	NP_001387267.1:n.988-656C>T
NM_001400339.1:c.911C>T	NP_001387268.1:p.Thr304Ile
NR_174476.1:n.1396C>T