Canonical Allele Identifier: CA1562889839
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90763274_90763275delinsTG , CM000667.2:g.90763274_90763275delinsTG GRCh38
NC_000005.9:g.90059091_90059092delinsTG , CM000667.1:g.90059091_90059092delinsTG GRCh37
NC_000005.8:g.90094847_90094848delinsTG NCBI36
NG_007083.1:g.209475_209476delinsTG
NG_007083.2:g.238931_238932delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.12121-31_12121-30delinsTG MANE Select ENSP00000384582.2:n.12121-31_12121-30delinsTG
ENST00000425867.3:c.1075-31_1075-30delinsTG ENSP00000392618.3:n.1075-31_1075-30delinsTG
ENST00000639431.1:c.265+87065_265+87066delinsTG ENSP00000491057.1:n.265+87065_265+87066delinsTG
ENST00000640464.1:n.2540-31_2540-30delinsTG
ENST00000640729.1:n.667_668delinsTG
ENST00000405460.6:c.12121-31_12121-30delinsTG ENSP00000384582.2:n.12121-31_12121-30delinsTG
NM_032119.3:c.12121-31_12121-30delinsTG NP_115495.3:n.12121-31_12121-30delinsTG
NR_003149.1:n.12134-31_12134-30delinsTG
XM_011543675.1:c.12118-31_12118-30delinsTG XP_011541977.1:n.12118-31_12118-30delinsTG
XM_011543676.1:c.12040-31_12040-30delinsTG XP_011541978.1:n.12040-31_12040-30delinsTG
XM_011543677.1:c.9424-31_9424-30delinsTG XP_011541979.1:n.9424-31_9424-30delinsTG
XM_011543678.1:c.12121-31_12121-30delinsTG XP_011541980.1:n.12121-31_12121-30delinsTG
NM_032119.4:c.12121-31_12121-30delinsTG MANE Select NP_115495.3:n.12121-31_12121-30delinsTG
XM_017009963.2:c.12142-31_12142-30delinsTG XP_016865452.1:n.12142-31_12142-30delinsTG
XM_017009964.2:c.12139-31_12139-30delinsTG XP_016865453.1:n.12139-31_12139-30delinsTG
XM_017009965.1:c.12139-31_12139-30delinsTG XP_016865454.1:n.12139-31_12139-30delinsTG
XM_017009966.2:c.12061-31_12061-30delinsTG XP_016865455.1:n.12061-31_12061-30delinsTG
XM_017009967.1:c.12046-31_12046-30delinsTG XP_016865456.1:n.12046-31_12046-30delinsTG
XM_017009968.2:c.12142-31_12142-30delinsTG XP_016865457.1:n.12142-31_12142-30delinsTG
XM_017009969.2:c.12142-31_12142-30delinsTG XP_016865458.1:n.12142-31_12142-30delinsTG
XM_017009970.2:c.12142-31_12142-30delinsTG XP_016865459.1:n.12142-31_12142-30delinsTG
XM_017009971.2:c.12142-31_12142-30delinsTG XP_016865460.1:n.12142-31_12142-30delinsTG
XM_017009972.1:c.5260-31_5260-30delinsTG XP_016865461.1:n.5260-31_5260-30delinsTG
XM_017009973.1:c.5239-31_5239-30delinsTG XP_016865462.1:n.5239-31_5239-30delinsTG
NR_003149.2:n.12137-31_12137-30delinsTG