Canonical Allele Identifier: CA360403390
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725648T>A , CM000667.2:g.90725648T>A GRCh38
NC_000005.9:g.90021465T>A , CM000667.1:g.90021465T>A GRCh37
NC_000005.8:g.90057221T>A NCBI36
NG_007083.1:g.171849T>A
NG_007083.2:g.201305T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10153T>A MANE Select ENSP00000384582.2:p.Leu3385Ile
ENST00000639431.1:c.265+49439T>A ENSP00000491057.1:n.265+49439T>A
ENST00000640374.1:n.3297T>A
ENST00000640464.1:n.572T>A
ENST00000405460.6:c.10153T>A ENSP00000384582.2:p.Leu3385Ile
ENST00000509621.1:c.2850T>A
NM_032119.3:c.10153T>A NP_115495.3:p.Leu3385Ile
NR_003149.1:n.10166T>A
XM_011543675.1:c.10150T>A XP_011541977.1:p.Leu3384Ile
XM_011543676.1:c.10072T>A XP_011541978.1:p.Leu3358Ile
XM_011543677.1:c.7456T>A XP_011541979.1:p.Leu2486Ile
XM_011543678.1:c.10153T>A XP_011541980.1:p.Leu3385Ile
XM_011543679.1:c.10153T>A XP_011541981.1:p.Leu3385Ile
XR_948560.1:n.272-9839A>T
NM_032119.4:c.10153T>A MANE Select NP_115495.3:p.Leu3385Ile
XM_017009963.2:c.10174T>A XP_016865452.1:p.Leu3392Ile
XM_017009964.2:c.10171T>A XP_016865453.1:p.Leu3391Ile
XM_017009965.1:c.10171T>A XP_016865454.1:p.Leu3391Ile
XM_017009966.2:c.10093T>A XP_016865455.1:p.Leu3365Ile
XM_017009967.1:c.10078T>A XP_016865456.1:p.Leu3360Ile
XM_017009968.2:c.10174T>A XP_016865457.1:p.Leu3392Ile
XM_017009969.2:c.10174T>A XP_016865458.1:p.Leu3392Ile
XM_017009970.2:c.10174T>A XP_016865459.1:p.Leu3392Ile
XM_017009971.2:c.10174T>A XP_016865460.1:p.Leu3392Ile
XM_017009972.1:c.3292T>A XP_016865461.1:p.Leu1098Ile
XM_017009973.1:c.3271T>A XP_016865462.1:p.Leu1091Ile
XM_017009974.2:c.10174T>A XP_016865463.1:p.Leu3392Ile
XR_001742802.1:n.2523-9839A>T
NR_003149.2:n.10169T>A