Canonical Allele Identifier: CA360425457
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823433A>G , CM000667.2:g.90823433A>G GRCh38
NC_000005.9:g.90119250A>G , CM000667.1:g.90119250A>G GRCh37
NC_000005.8:g.90155006A>G NCBI36
NG_007083.1:g.269634A>G
NG_007083.2:g.299090A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16205A>G MANE Select ENSP00000384582.2:p.Glu5402Gly
ENST00000425867.3:c.5159A>G ENSP00000392618.3:p.Glu1720Gly
ENST00000638510.1:n.3472A>G
ENST00000639431.1:c.265+147224A>G ENSP00000491057.1:n.265+147224A>G
ENST00000640061.1:n.128+1251A>G
ENST00000640407.1:c.2615A>G ENSP00000491425.1:p.Glu872Gly
ENST00000405460.6:c.16205A>G ENSP00000384582.2:p.Glu5402Gly
ENST00000425867.2:c.3188A>G ENSP00000392618.2:p.Glu1063Gly
NM_032119.3:c.16205A>G NP_115495.3:p.Glu5402Gly
NR_003149.1:n.16218A>G
XM_011543675.1:c.16202A>G XP_011541977.1:p.Glu5401Gly
XM_011543676.1:c.16124A>G XP_011541978.1:p.Glu5375Gly
XM_011543677.1:c.13508A>G XP_011541979.1:p.Glu4503Gly
NM_032119.4:c.16205A>G MANE Select NP_115495.3:p.Glu5402Gly
XM_017009963.2:c.16226A>G XP_016865452.1:p.Glu5409Gly
XM_017009964.2:c.16223A>G XP_016865453.1:p.Glu5408Gly
XM_017009965.1:c.16223A>G XP_016865454.1:p.Glu5408Gly
XM_017009966.2:c.16145A>G XP_016865455.1:p.Glu5382Gly
XM_017009967.1:c.16130A>G XP_016865456.1:p.Glu5377Gly
XM_017009968.2:c.16046A>G XP_016865457.1:p.Glu5349Gly
XM_017009969.2:c.16226A>G XP_016865458.1:p.Glu5409Gly
XM_017009972.1:c.9344A>G XP_016865461.1:p.Glu3115Gly
XM_017009973.1:c.9323A>G XP_016865462.1:p.Glu3108Gly
NR_003149.2:n.16221A>G