Canonical Allele Identifier: CA261829
Gene: ADGRV1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90728736_90728738dup , CM000667.2:g.90728736_90728738dup GRCh38
NC_000005.9:g.90024553_90024555dup , CM000667.1:g.90024553_90024555dup GRCh37
NC_000005.8:g.90060309_90060311dup NCBI36
NG_007083.1:g.174937_174939dup
NG_007083.2:g.204393_204395dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10229_10231dup MANE Select ENSP00000384582.2:p.Val3410_Ala3411insVal
ENST00000639431.1:c.265+52527_265+52529dup ENSP00000491057.1:n.265+52527_265+52529dup
ENST00000640374.1:n.3373_3375dup
ENST00000640464.1:n.648_650dup
ENST00000405460.6:c.10229_10231dup ENSP00000384582.2:p.Val3410_Ala3411insVal
ENST00000509621.1:c.2926_2928dup
NM_032119.3:c.10229_10231dup NP_115495.3:p.Val3410_Ala3411insVal
NR_003149.1:n.10242_10244dup
XM_011543675.1:c.10226_10228dup XP_011541977.1:p.Val3409_Ala3410insVal
XM_011543676.1:c.10148_10150dup XP_011541978.1:p.Val3383_Ala3384insVal
XM_011543677.1:c.7532_7534dup XP_011541979.1:p.Val2511_Ala2512insVal
XM_011543678.1:c.10229_10231dup XP_011541980.1:p.Val3410_Ala3411insVal
XM_011543679.1:c.10229_10231dup XP_011541981.1:p.Val3410_Ala3411insVal
XR_948560.1:n.271+12170_271+12172dup
NM_032119.4:c.10229_10231dup MANE Select NP_115495.3:p.Val3410_Ala3411insVal
XM_017009963.2:c.10250_10252dup XP_016865452.1:p.Val3417_Ala3418insVal
XM_017009964.2:c.10247_10249dup XP_016865453.1:p.Val3416_Ala3417insVal
XM_017009965.1:c.10247_10249dup XP_016865454.1:p.Val3416_Ala3417insVal
XM_017009966.2:c.10169_10171dup XP_016865455.1:p.Val3390_Ala3391insVal
XM_017009967.1:c.10154_10156dup XP_016865456.1:p.Val3385_Ala3386insVal
XM_017009968.2:c.10250_10252dup XP_016865457.1:p.Val3417_Ala3418insVal
XM_017009969.2:c.10250_10252dup XP_016865458.1:p.Val3417_Ala3418insVal
XM_017009970.2:c.10250_10252dup XP_016865459.1:p.Val3417_Ala3418insVal
XM_017009971.2:c.10250_10252dup XP_016865460.1:p.Val3417_Ala3418insVal
XM_017009972.1:c.3368_3370dup XP_016865461.1:p.Val1123_Ala1124insVal
XM_017009973.1:c.3347_3349dup XP_016865462.1:p.Val1116_Ala1117insVal
XM_017009974.2:c.10250_10252dup XP_016865463.1:p.Val3417_Ala3418insVal
XR_001742802.1:n.2522+12170_2522+12172dup
NR_003149.2:n.10245_10247dup
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