Canonical Allele Identifier: CA360397422
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716614T>A , CM000667.2:g.90716614T>A GRCh38
NC_000005.9:g.90012431T>A , CM000667.1:g.90012431T>A GRCh37
NC_000005.8:g.90048187T>A NCBI36
NG_007083.1:g.162815T>A
NG_007083.2:g.192271T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9332T>A MANE Select ENSP00000384582.2:p.Leu3111Ter
ENST00000639431.1:c.265+40405T>A ENSP00000491057.1:n.265+40405T>A
ENST00000639473.1:n.4791T>A
ENST00000640012.1:c.3139T>A
ENST00000640374.1:n.2476T>A
ENST00000640779.1:c.4061T>A
ENST00000405460.6:c.9332T>A ENSP00000384582.2:p.Leu3111Ter
ENST00000509621.1:c.2029T>A
NM_032119.3:c.9332T>A NP_115495.3:p.Leu3111Ter
NR_003149.1:n.9345T>A
XM_011543675.1:c.9329T>A XP_011541977.1:p.Leu3110Ter
XM_011543676.1:c.9251T>A XP_011541978.1:p.Leu3084Ter
XM_011543677.1:c.6635T>A XP_011541979.1:p.Leu2212Ter
XM_011543678.1:c.9332T>A XP_011541980.1:p.Leu3111Ter
XM_011543679.1:c.9332T>A XP_011541981.1:p.Leu3111Ter
XR_948560.1:n.272-805A>T
NM_032119.4:c.9332T>A MANE Select NP_115495.3:p.Leu3111Ter
XM_017009963.2:c.9353T>A XP_016865452.1:p.Leu3118Ter
XM_017009964.2:c.9350T>A XP_016865453.1:p.Leu3117Ter
XM_017009965.1:c.9350T>A XP_016865454.1:p.Leu3117Ter
XM_017009966.2:c.9272T>A XP_016865455.1:p.Leu3091Ter
XM_017009967.1:c.9257T>A XP_016865456.1:p.Leu3086Ter
XM_017009968.2:c.9353T>A XP_016865457.1:p.Leu3118Ter
XM_017009969.2:c.9353T>A XP_016865458.1:p.Leu3118Ter
XM_017009970.2:c.9353T>A XP_016865459.1:p.Leu3118Ter
XM_017009971.2:c.9353T>A XP_016865460.1:p.Leu3118Ter
XM_017009972.1:c.2471T>A XP_016865461.1:p.Leu824Ter
XM_017009973.1:c.2450T>A XP_016865462.1:p.Leu817Ter
XM_017009974.2:c.9353T>A XP_016865463.1:p.Leu3118Ter
XR_001742802.1:n.2523-805A>T
NR_003149.2:n.9348T>A