Canonical Allele Identifier: CA360366837
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755090C>A , CM000667.2:g.90755090C>A GRCh38
NC_000005.9:g.90050907C>A , CM000667.1:g.90050907C>A GRCh37
NC_000005.8:g.90086663C>A NCBI36
NG_007083.1:g.201291C>A
NG_007083.2:g.230747C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11485C>A MANE Select ENSP00000384582.2:p.Gln3829Lys
ENST00000425867.3:c.616C>A ENSP00000392618.3:p.Gln206Lys
ENST00000639431.1:c.265+78881C>A ENSP00000491057.1:n.265+78881C>A
ENST00000640374.1:n.4629C>A
ENST00000640464.1:n.1904C>A
ENST00000405460.6:c.11485C>A ENSP00000384582.2:p.Gln3829Lys
ENST00000509621.1:c.4182C>A
NM_032119.3:c.11485C>A NP_115495.3:p.Gln3829Lys
NR_003149.1:n.11498C>A
XM_011543675.1:c.11482C>A XP_011541977.1:p.Gln3828Lys
XM_011543676.1:c.11404C>A XP_011541978.1:p.Gln3802Lys
XM_011543677.1:c.8788C>A XP_011541979.1:p.Gln2930Lys
XM_011543678.1:c.11485C>A XP_011541980.1:p.Gln3829Lys
NM_032119.4:c.11485C>A MANE Select NP_115495.3:p.Gln3829Lys
XM_017009963.2:c.11506C>A XP_016865452.1:p.Gln3836Lys
XM_017009964.2:c.11503C>A XP_016865453.1:p.Gln3835Lys
XM_017009965.1:c.11503C>A XP_016865454.1:p.Gln3835Lys
XM_017009966.2:c.11425C>A XP_016865455.1:p.Gln3809Lys
XM_017009967.1:c.11410C>A XP_016865456.1:p.Gln3804Lys
XM_017009968.2:c.11506C>A XP_016865457.1:p.Gln3836Lys
XM_017009969.2:c.11506C>A XP_016865458.1:p.Gln3836Lys
XM_017009970.2:c.11506C>A XP_016865459.1:p.Gln3836Lys
XM_017009971.2:c.11506C>A XP_016865460.1:p.Gln3836Lys
XM_017009972.1:c.4624C>A XP_016865461.1:p.Gln1542Lys
XM_017009973.1:c.4603C>A XP_016865462.1:p.Gln1535Lys
NR_003149.2:n.11501C>A