Canonical Allele Identifier: CA360366934
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755105G>C , CM000667.2:g.90755105G>C GRCh38
NC_000005.9:g.90050922G>C , CM000667.1:g.90050922G>C GRCh37
NC_000005.8:g.90086678G>C NCBI36
NG_007083.1:g.201306G>C
NG_007083.2:g.230762G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11500G>C MANE Select ENSP00000384582.2:p.Glu3834Gln
ENST00000425867.3:c.631G>C ENSP00000392618.3:p.Glu211Gln
ENST00000639431.1:c.265+78896G>C ENSP00000491057.1:n.265+78896G>C
ENST00000640374.1:n.4644G>C
ENST00000640464.1:n.1919G>C
ENST00000405460.6:c.11500G>C ENSP00000384582.2:p.Glu3834Gln
ENST00000509621.1:c.4197G>C
NM_032119.3:c.11500G>C NP_115495.3:p.Glu3834Gln
NR_003149.1:n.11513G>C
XM_011543675.1:c.11497G>C XP_011541977.1:p.Glu3833Gln
XM_011543676.1:c.11419G>C XP_011541978.1:p.Glu3807Gln
XM_011543677.1:c.8803G>C XP_011541979.1:p.Glu2935Gln
XM_011543678.1:c.11500G>C XP_011541980.1:p.Glu3834Gln
NM_032119.4:c.11500G>C MANE Select NP_115495.3:p.Glu3834Gln
XM_017009963.2:c.11521G>C XP_016865452.1:p.Glu3841Gln
XM_017009964.2:c.11518G>C XP_016865453.1:p.Glu3840Gln
XM_017009965.1:c.11518G>C XP_016865454.1:p.Glu3840Gln
XM_017009966.2:c.11440G>C XP_016865455.1:p.Glu3814Gln
XM_017009967.1:c.11425G>C XP_016865456.1:p.Glu3809Gln
XM_017009968.2:c.11521G>C XP_016865457.1:p.Glu3841Gln
XM_017009969.2:c.11521G>C XP_016865458.1:p.Glu3841Gln
XM_017009970.2:c.11521G>C XP_016865459.1:p.Glu3841Gln
XM_017009971.2:c.11521G>C XP_016865460.1:p.Glu3841Gln
XM_017009972.1:c.4639G>C XP_016865461.1:p.Glu1547Gln
XM_017009973.1:c.4618G>C XP_016865462.1:p.Glu1540Gln
NR_003149.2:n.11516G>C