Canonical Allele Identifier: CA13356312
Gene: VTI1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112628513A>G , CM000672.2:g.112628513A>G GRCh38
NC_000010.10:g.114388272A>G , CM000672.1:g.114388272A>G GRCh37
NC_000010.9:g.114378262A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000705995.1:c.449-39705A>G ENSP00000516199.1:n.449-39705A>G
ENST00000393077.3:c.428-39705A>G MANE Select ENSP00000376792.2:n.428-39705A>G
ENST00000393077.2:c.428-39705A>G ENSP00000376792.2:n.428-39705A>G
ENST00000432306.5:c.428-39705A>G ENSP00000395017.1:n.428-39705A>G
NM_145206.2:c.428-39705A>G NP_660207.2:n.428-39705A>G
XM_005269543.3:c.449-39705A>G XP_005269600.1:n.449-39705A>G
XM_005269544.3:c.428-39705A>G XP_005269601.1:n.428-39705A>G
XM_005269545.3:c.449-39705A>G XP_005269602.1:n.449-39705A>G
XM_005269546.2:c.449-39705A>G XP_005269603.1:n.449-39705A>G
XM_005269547.3:c.428-39705A>G XP_005269604.1:n.428-39705A>G
XM_005269548.1:c.428-39705A>G XP_005269605.1:n.428-39705A>G
XM_006717636.2:c.449-39705A>G XP_006717699.1:n.449-39705A>G
XM_006717637.1:c.449-39705A>G XP_006717700.1:n.449-39705A>G
XM_011539328.1:c.449-39705A>G XP_011537630.1:n.449-39705A>G
XM_011539329.1:c.428-39705A>G XP_011537631.1:n.428-39705A>G
XM_011539330.1:c.449-39705A>G XP_011537632.1:n.449-39705A>G
XM_011539331.1:c.449-39705A>G XP_011537633.1:n.449-39705A>G
XM_011539332.1:c.449-39705A>G XP_011537634.1:n.449-39705A>G
NM_001318203.1:c.449-39705A>G NP_001305132.1:n.449-39705A>G
NM_001318205.1:c.428-39705A>G NP_001305134.1:n.428-39705A>G
NM_001365710.1:c.428-39705A>G NP_001352639.1:n.428-39705A>G
NM_001365711.1:c.449-39705A>G NP_001352640.1:n.449-39705A>G
NM_001365712.1:c.449-39705A>G NP_001352641.1:n.449-39705A>G
NM_001365713.1:c.449-39705A>G NP_001352642.1:n.449-39705A>G
NM_001365714.1:c.428-39705A>G NP_001352643.1:n.428-39705A>G
NM_145206.3:c.428-39705A>G NP_660207.2:n.428-39705A>G
XM_005269545.5:c.449-39705A>G XP_005269602.1:n.449-39705A>G
XM_011539328.3:c.449-39705A>G XP_011537630.1:n.449-39705A>G
XM_011539330.3:c.449-39705A>G XP_011537632.1:n.449-39705A>G
XM_017015745.2:c.449-39705A>G XP_016871234.1:n.449-39705A>G
XM_017015746.2:c.428-39705A>G XP_016871235.1:n.428-39705A>G
XM_017015747.2:c.449-39705A>G XP_016871236.1:n.449-39705A>G
XM_017015748.2:c.428-39705A>G XP_016871237.1:n.428-39705A>G
XR_002956958.1:n.824-39705A>G
NM_001365710.2:c.428-39705A>G NP_001352639.1:n.428-39705A>G
NM_001318203.2:c.449-39705A>G NP_001305132.1:n.449-39705A>G
NM_001318205.2:c.428-39705A>G NP_001305134.1:n.428-39705A>G
NM_145206.4:c.428-39705A>G MANE Select NP_660207.2:n.428-39705A>G