Canonical Allele Identifier: CA360403205
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725570G>C , CM000667.2:g.90725570G>C GRCh38
NC_000005.9:g.90021387G>C , CM000667.1:g.90021387G>C GRCh37
NC_000005.8:g.90057143G>C NCBI36
NG_007083.1:g.171771G>C
NG_007083.2:g.201227G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10075G>C MANE Select ENSP00000384582.2:p.Glu3359Gln
ENST00000639431.1:c.265+49361G>C ENSP00000491057.1:n.265+49361G>C
ENST00000640374.1:n.3219G>C
ENST00000640464.1:n.494G>C
ENST00000405460.6:c.10075G>C ENSP00000384582.2:p.Glu3359Gln
ENST00000509621.1:c.2772G>C
NM_032119.3:c.10075G>C NP_115495.3:p.Glu3359Gln
NR_003149.1:n.10088G>C
XM_011543675.1:c.10072G>C XP_011541977.1:p.Glu3358Gln
XM_011543676.1:c.9994G>C XP_011541978.1:p.Glu3332Gln
XM_011543677.1:c.7378G>C XP_011541979.1:p.Glu2460Gln
XM_011543678.1:c.10075G>C XP_011541980.1:p.Glu3359Gln
XM_011543679.1:c.10075G>C XP_011541981.1:p.Glu3359Gln
XR_948560.1:n.272-9761C>G
NM_032119.4:c.10075G>C MANE Select NP_115495.3:p.Glu3359Gln
XM_017009963.2:c.10096G>C XP_016865452.1:p.Glu3366Gln
XM_017009964.2:c.10093G>C XP_016865453.1:p.Glu3365Gln
XM_017009965.1:c.10093G>C XP_016865454.1:p.Glu3365Gln
XM_017009966.2:c.10015G>C XP_016865455.1:p.Glu3339Gln
XM_017009967.1:c.10000G>C XP_016865456.1:p.Glu3334Gln
XM_017009968.2:c.10096G>C XP_016865457.1:p.Glu3366Gln
XM_017009969.2:c.10096G>C XP_016865458.1:p.Glu3366Gln
XM_017009970.2:c.10096G>C XP_016865459.1:p.Glu3366Gln
XM_017009971.2:c.10096G>C XP_016865460.1:p.Glu3366Gln
XM_017009972.1:c.3214G>C XP_016865461.1:p.Glu1072Gln
XM_017009973.1:c.3193G>C XP_016865462.1:p.Glu1065Gln
XM_017009974.2:c.10096G>C XP_016865463.1:p.Glu3366Gln
XR_001742802.1:n.2523-9761C>G
NR_003149.2:n.10091G>C