Canonical Allele Identifier: CA1562918424
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs1763825173

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823782_90823783insACAAG , CM000667.2:g.90823782_90823783insACAAG GRCh38
NC_000005.9:g.90119599_90119600insACAAG , CM000667.1:g.90119599_90119600insACAAG GRCh37
NC_000005.8:g.90155355_90155356insACAAG NCBI36
NG_007083.1:g.269983_269984insACAAG
NG_007083.2:g.299439_299440insACAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16368+186_16368+187insACAAG MANE Select ENSP00000384582.2:n.16368+186_16368+187insACAAG
ENST00000425867.3:c.5322+186_5322+187insACAAG ENSP00000392618.3:n.5322+186_5322+187insACAAG
ENST00000638510.1:n.3635+186_3635+187insACAAG
ENST00000639431.1:c.265+147573_265+147574insACAAG ENSP00000491057.1:n.265+147573_265+147574insACAAG
ENST00000640061.1:n.128+1600_128+1601insACAAG
ENST00000640407.1:c.2778+186_2778+187insACAAG ENSP00000491425.1:n.2778+186_2778+187insACAAG
ENST00000405460.6:c.16368+186_16368+187insACAAG ENSP00000384582.2:n.16368+186_16368+187insACAAG
ENST00000425867.2:c.3351+186_3351+187insACAAG ENSP00000392618.2:n.3351+186_3351+187insACAAG
NM_032119.3:c.16368+186_16368+187insACAAG NP_115495.3:n.16368+186_16368+187insACAAG
NR_003149.1:n.16381+186_16381+187insACAAG
XM_011543675.1:c.16365+186_16365+187insACAAG XP_011541977.1:n.16365+186_16365+187insACAAG
XM_011543676.1:c.16287+186_16287+187insACAAG XP_011541978.1:n.16287+186_16287+187insACAAG
XM_011543677.1:c.13671+186_13671+187insACAAG XP_011541979.1:n.13671+186_13671+187insACAAG
NM_032119.4:c.16368+186_16368+187insACAAG MANE Select NP_115495.3:n.16368+186_16368+187insACAAG
XM_017009963.2:c.16389+186_16389+187insACAAG XP_016865452.1:n.16389+186_16389+187insACAAG
XM_017009964.2:c.16386+186_16386+187insACAAG XP_016865453.1:n.16386+186_16386+187insACAAG
XM_017009965.1:c.16386+186_16386+187insACAAG XP_016865454.1:n.16386+186_16386+187insACAAG
XM_017009966.2:c.16308+186_16308+187insACAAG XP_016865455.1:n.16308+186_16308+187insACAAG
XM_017009967.1:c.16293+186_16293+187insACAAG XP_016865456.1:n.16293+186_16293+187insACAAG
XM_017009968.2:c.16209+186_16209+187insACAAG XP_016865457.1:n.16209+186_16209+187insACAAG
XM_017009969.2:c.16389+186_16389+187insACAAG XP_016865458.1:n.16389+186_16389+187insACAAG
XM_017009972.1:c.9507+186_9507+187insACAAG XP_016865461.1:n.9507+186_9507+187insACAAG
XM_017009973.1:c.9486+186_9486+187insACAAG XP_016865462.1:n.9486+186_9486+187insACAAG
NR_003149.2:n.16384+186_16384+187insACAAG