Canonical Allele Identifier: CA13229313
Gene: VTI1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112738717G>A , CM000672.2:g.112738717G>A GRCh38
NC_000010.10:g.114498476G>A , CM000672.1:g.114498476G>A GRCh37
NC_000010.9:g.114488466G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000705995.1:c.581+69719G>A ENSP00000516199.1:n.581+69719G>A
ENST00000393077.3:c.560+69719G>A MANE Select ENSP00000376792.2:n.560+69719G>A
ENST00000393077.2:c.560+69719G>A ENSP00000376792.2:n.560+69719G>A
NM_145206.2:c.560+69719G>A NP_660207.2:n.560+69719G>A
XM_005269543.3:c.581+69719G>A XP_005269600.1:n.581+69719G>A
XM_005269545.3:c.582-13636G>A XP_005269602.1:n.582-13636G>A
XM_005269546.2:c.*7+69708G>A XP_005269603.1:n.*7+69708G>A
XM_005269547.3:c.561-13636G>A XP_005269604.1:n.561-13636G>A
XM_005269548.1:c.*7+69708G>A XP_005269605.1:n.*7+69708G>A
XM_006717637.1:c.581+69719G>A XP_006717700.1:n.581+69719G>A
XM_011539331.1:c.*7+69708G>A XP_011537633.1:n.*7+69708G>A
NM_001318203.1:c.581+69719G>A NP_001305132.1:n.581+69719G>A
NM_001318205.1:c.*7+69708G>A NP_001305134.1:n.*7+69708G>A
NM_001365711.1:c.581+69719G>A NP_001352640.1:n.581+69719G>A
NM_001365712.1:c.*7+69708G>A NP_001352641.1:n.*7+69708G>A
NM_001365713.1:c.*7+69708G>A NP_001352642.1:n.*7+69708G>A
NM_001365714.1:c.561-13636G>A NP_001352643.1:n.561-13636G>A
NM_145206.3:c.560+69719G>A NP_660207.2:n.560+69719G>A
XM_005269545.5:c.582-13636G>A XP_005269602.1:n.582-13636G>A
XM_011539330.3:c.*1943G>A XP_011537632.1:n.*1943G>A
XM_017015745.2:c.582-43461G>A XP_016871234.1:n.582-43461G>A
XM_017015746.2:c.561-43461G>A XP_016871235.1:n.561-43461G>A
XM_017015747.2:c.581+69719G>A XP_016871236.1:n.581+69719G>A
XM_017015748.2:c.560+69719G>A XP_016871237.1:n.560+69719G>A
XR_002956958.1:n.956+69719G>A
NM_001318203.2:c.581+69719G>A NP_001305132.1:n.581+69719G>A
NM_001318205.2:c.*7+69708G>A NP_001305134.1:n.*7+69708G>A
NM_145206.4:c.560+69719G>A MANE Select NP_660207.2:n.560+69719G>A
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