Canonical Allele Identifier: CA1562918416
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs1763823905

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823775_90823776insCAACT , CM000667.2:g.90823775_90823776insCAACT GRCh38
NC_000005.9:g.90119592_90119593insCAACT , CM000667.1:g.90119592_90119593insCAACT GRCh37
NC_000005.8:g.90155348_90155349insCAACT NCBI36
NG_007083.1:g.269976_269977insCAACT
NG_007083.2:g.299432_299433insCAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16368+179_16368+180insCAACT MANE Select ENSP00000384582.2:n.16368+179_16368+180insCAACT
ENST00000425867.3:c.5322+179_5322+180insCAACT ENSP00000392618.3:n.5322+179_5322+180insCAACT
ENST00000638510.1:n.3635+179_3635+180insCAACT
ENST00000639431.1:c.265+147566_265+147567insCAACT ENSP00000491057.1:n.265+147566_265+147567insCAACT
ENST00000640061.1:n.128+1593_128+1594insCAACT
ENST00000640407.1:c.2778+179_2778+180insCAACT ENSP00000491425.1:n.2778+179_2778+180insCAACT
ENST00000405460.6:c.16368+179_16368+180insCAACT ENSP00000384582.2:n.16368+179_16368+180insCAACT
ENST00000425867.2:c.3351+179_3351+180insCAACT ENSP00000392618.2:n.3351+179_3351+180insCAACT
NM_032119.3:c.16368+179_16368+180insCAACT NP_115495.3:n.16368+179_16368+180insCAACT
NR_003149.1:n.16381+179_16381+180insCAACT
XM_011543675.1:c.16365+179_16365+180insCAACT XP_011541977.1:n.16365+179_16365+180insCAACT
XM_011543676.1:c.16287+179_16287+180insCAACT XP_011541978.1:n.16287+179_16287+180insCAACT
XM_011543677.1:c.13671+179_13671+180insCAACT XP_011541979.1:n.13671+179_13671+180insCAACT
NM_032119.4:c.16368+179_16368+180insCAACT MANE Select NP_115495.3:n.16368+179_16368+180insCAACT
XM_017009963.2:c.16389+179_16389+180insCAACT XP_016865452.1:n.16389+179_16389+180insCAACT
XM_017009964.2:c.16386+179_16386+180insCAACT XP_016865453.1:n.16386+179_16386+180insCAACT
XM_017009965.1:c.16386+179_16386+180insCAACT XP_016865454.1:n.16386+179_16386+180insCAACT
XM_017009966.2:c.16308+179_16308+180insCAACT XP_016865455.1:n.16308+179_16308+180insCAACT
XM_017009967.1:c.16293+179_16293+180insCAACT XP_016865456.1:n.16293+179_16293+180insCAACT
XM_017009968.2:c.16209+179_16209+180insCAACT XP_016865457.1:n.16209+179_16209+180insCAACT
XM_017009969.2:c.16389+179_16389+180insCAACT XP_016865458.1:n.16389+179_16389+180insCAACT
XM_017009972.1:c.9507+179_9507+180insCAACT XP_016865461.1:n.9507+179_9507+180insCAACT
XM_017009973.1:c.9486+179_9486+180insCAACT XP_016865462.1:n.9486+179_9486+180insCAACT
NR_003149.2:n.16384+179_16384+180insCAACT