Canonical Allele Identifier: CA360425511
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823459A>G , CM000667.2:g.90823459A>G GRCh38
NC_000005.9:g.90119276A>G , CM000667.1:g.90119276A>G GRCh37
NC_000005.8:g.90155032A>G NCBI36
NG_007083.1:g.269660A>G
NG_007083.2:g.299116A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16231A>G MANE Select ENSP00000384582.2:p.Thr5411Ala
ENST00000425867.3:c.5185A>G ENSP00000392618.3:p.Thr1729Ala
ENST00000638510.1:n.3498A>G
ENST00000639431.1:c.265+147250A>G ENSP00000491057.1:n.265+147250A>G
ENST00000640061.1:n.128+1277A>G
ENST00000640407.1:c.2641A>G ENSP00000491425.1:p.Thr881Ala
ENST00000405460.6:c.16231A>G ENSP00000384582.2:p.Thr5411Ala
ENST00000425867.2:c.3214A>G ENSP00000392618.2:p.Thr1072Ala
NM_032119.3:c.16231A>G NP_115495.3:p.Thr5411Ala
NR_003149.1:n.16244A>G
XM_011543675.1:c.16228A>G XP_011541977.1:p.Thr5410Ala
XM_011543676.1:c.16150A>G XP_011541978.1:p.Thr5384Ala
XM_011543677.1:c.13534A>G XP_011541979.1:p.Thr4512Ala
NM_032119.4:c.16231A>G MANE Select NP_115495.3:p.Thr5411Ala
XM_017009963.2:c.16252A>G XP_016865452.1:p.Thr5418Ala
XM_017009964.2:c.16249A>G XP_016865453.1:p.Thr5417Ala
XM_017009965.1:c.16249A>G XP_016865454.1:p.Thr5417Ala
XM_017009966.2:c.16171A>G XP_016865455.1:p.Thr5391Ala
XM_017009967.1:c.16156A>G XP_016865456.1:p.Thr5386Ala
XM_017009968.2:c.16072A>G XP_016865457.1:p.Thr5358Ala
XM_017009969.2:c.16252A>G XP_016865458.1:p.Thr5418Ala
XM_017009972.1:c.9370A>G XP_016865461.1:p.Thr3124Ala
XM_017009973.1:c.9349A>G XP_016865462.1:p.Thr3117Ala
NR_003149.2:n.16247A>G