Canonical Allele Identifier: CA445404124
Gene: ADGRV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.90050924A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755107A>G , CM000667.2:g.90755107A>G GRCh38
NC_000005.9:g.90050924A>G , CM000667.1:g.90050924A>G GRCh37
NC_000005.8:g.90086680A>G NCBI36
NG_007083.1:g.201308A>G
NG_007083.2:g.230764A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11502A>G MANE Select ENSP00000384582.2:p.Glu3834=
ENST00000425867.3:c.633A>G ENSP00000392618.3:p.Glu211=
ENST00000639431.1:c.265+78898A>G ENSP00000491057.1:n.265+78898A>G
ENST00000640374.1:n.4646A>G
ENST00000640464.1:n.1921A>G
ENST00000405460.6:c.11502A>G ENSP00000384582.2:p.Glu3834=
ENST00000509621.1:c.4199A>G
NM_032119.3:c.11502A>G NP_115495.3:p.Glu3834=
NR_003149.1:n.11515A>G
XM_011543675.1:c.11499A>G XP_011541977.1:p.Glu3833=
XM_011543676.1:c.11421A>G XP_011541978.1:p.Glu3807=
XM_011543677.1:c.8805A>G XP_011541979.1:p.Glu2935=
XM_011543678.1:c.11502A>G XP_011541980.1:p.Glu3834=
NM_032119.4:c.11502A>G MANE Select NP_115495.3:p.Glu3834=
XM_017009963.2:c.11523A>G XP_016865452.1:p.Glu3841=
XM_017009964.2:c.11520A>G XP_016865453.1:p.Glu3840=
XM_017009965.1:c.11520A>G XP_016865454.1:p.Glu3840=
XM_017009966.2:c.11442A>G XP_016865455.1:p.Glu3814=
XM_017009967.1:c.11427A>G XP_016865456.1:p.Glu3809=
XM_017009968.2:c.11523A>G XP_016865457.1:p.Glu3841=
XM_017009969.2:c.11523A>G XP_016865458.1:p.Glu3841=
XM_017009970.2:c.11523A>G XP_016865459.1:p.Glu3841=
XM_017009971.2:c.11523A>G XP_016865460.1:p.Glu3841=
XM_017009972.1:c.4641A>G XP_016865461.1:p.Glu1547=
XM_017009973.1:c.4620A>G XP_016865462.1:p.Glu1540=
NR_003149.2:n.11518A>G