Canonical Allele Identifier: CA113867

Gene: VIPAS39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77435885G>A , CM000676.2:g.77435885G>A	GRCh38
NC_000014.8:g.77902228G>A , CM000676.1:g.77902228G>A	GRCh37
NC_000014.7:g.76971981G>A	NCBI36
NG_023421.1:g.26756C>T
NG_023421.2:g.26756C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001193315.2:c.871C>T MANE Select	NP_001180244.1:p.Gln291Ter
ENST00000557658.6:c.871C>T MANE Select	ENSP00000452191.1:p.Gln291Ter
NM_001193314.1:c.871C>T	NP_001180243.1:p.Gln291Ter
NM_001193314.2:c.871C>T	NP_001180243.1:p.Gln291Ter
NM_001193315.1:c.871C>T	NP_001180244.1:p.Gln291Ter
NM_001193316.1:c.724C>T	NP_001180245.1:p.Gln242Ter
NM_001193316.2:c.724C>T	NP_001180245.1:p.Gln242Ter
NM_001193317.1:c.871C>T	NP_001180246.1:p.Gln291Ter
NM_001193317.2:c.871C>T	NP_001180246.1:p.Gln291Ter
NM_001400324.1:c.724C>T	NP_001387253.1:p.Gln242Ter
NM_001400325.1:c.724C>T	NP_001387254.1:p.Gln242Ter
NM_001400326.1:c.871C>T	NP_001387255.1:p.Gln291Ter
NM_001400327.1:c.838C>T	NP_001387256.1:p.Gln280Ter
NM_001400330.1:c.871C>T	NP_001387259.1:p.Gln291Ter
NM_001400331.1:c.871C>T	NP_001387260.1:p.Gln291Ter
NM_001400332.1:c.871C>T	NP_001387261.1:p.Gln291Ter
NM_001400333.1:c.778C>T	NP_001387262.1:p.Gln260Ter
NM_001400334.1:c.778C>T	NP_001387263.1:p.Gln260Ter
NM_001400335.1:c.871C>T	NP_001387264.1:p.Gln291Ter
NM_001400336.1:c.871C>T	NP_001387265.1:p.Gln291Ter
NM_001400337.1:c.631C>T	NP_001387266.1:p.Gln211Ter
NM_001400338.1:c.769C>T	NP_001387267.1:p.Gln257Ter
NM_001400339.1:c.763-1582C>T	NP_001387268.1:n.763-1582C>T
NM_022067.3:c.871C>T	NP_071350.2:p.Gln291Ter
NM_022067.4:c.871C>T	NP_071350.2:p.Gln291Ter
NR_174476.1:n.978C>T
ENST00000327028.8:c.724C>T	ENSP00000313098.5:p.Gln242Ter
ENST00000343765.6:c.871C>T	ENSP00000339122.2:p.Gln291Ter
ENST00000448935.6:c.724C>T	ENSP00000404815.2:p.Gln242Ter
ENST00000553576.5:n.283C>T
ENST00000553888.5:c.871C>T	ENSP00000452181.1:p.Gln291Ter
ENST00000556412.4:c.949C>T	ENSP00000451857.1:p.Gln317Ter
ENST00000557658.5:c.871C>T	ENSP00000452191.1:p.Gln291Ter
XM_011537066.1:c.778C>T	XP_011535368.1:p.Gln260Ter
XM_011537066.2:c.778C>T	XP_011535368.1:p.Gln260Ter
XM_017021580.2:c.871C>T	XP_016877069.1:p.Gln291Ter
XM_017021581.2:c.871C>T	XP_016877070.1:p.Gln291Ter
XM_024449688.1:c.778C>T	XP_024305456.1:p.Gln260Ter
XR_001750501.2:n.993C>T