Canonical Allele Identifier: CA360372026
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692770A>T , CM000667.2:g.90692770A>T GRCh38
NC_000005.9:g.89988587A>T , CM000667.1:g.89988587A>T GRCh37
NC_000005.8:g.90024343A>T NCBI36
NG_007083.1:g.138971A>T
NG_007083.2:g.168427A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7117A>T MANE Select ENSP00000384582.2:p.Ile2373Leu
ENST00000639431.1:c.265+16561A>T ENSP00000491057.1:n.265+16561A>T
ENST00000639473.1:n.2576A>T
ENST00000640012.1:c.924A>T
ENST00000640374.1:n.261A>T
ENST00000640403.1:c.4408A>T ENSP00000492531.1:p.Ile1470Leu
ENST00000640779.1:c.1846A>T
ENST00000405460.6:c.7117A>T ENSP00000384582.2:p.Ile2373Leu
NM_032119.3:c.7117A>T NP_115495.3:p.Ile2373Leu
NR_003149.1:n.7130A>T
XM_011543675.1:c.7114A>T XP_011541977.1:p.Ile2372Leu
XM_011543676.1:c.7036A>T XP_011541978.1:p.Ile2346Leu
XM_011543677.1:c.4420A>T XP_011541979.1:p.Ile1474Leu
XM_011543678.1:c.7117A>T XP_011541980.1:p.Ile2373Leu
XM_011543679.1:c.7117A>T XP_011541981.1:p.Ile2373Leu
NM_032119.4:c.7117A>T MANE Select NP_115495.3:p.Ile2373Leu
XM_017009963.2:c.7117A>T XP_016865452.1:p.Ile2373Leu
XM_017009964.2:c.7114A>T XP_016865453.1:p.Ile2372Leu
XM_017009965.1:c.7114A>T XP_016865454.1:p.Ile2372Leu
XM_017009966.2:c.7036A>T XP_016865455.1:p.Ile2346Leu
XM_017009967.1:c.7021A>T XP_016865456.1:p.Ile2341Leu
XM_017009968.2:c.7117A>T XP_016865457.1:p.Ile2373Leu
XM_017009969.2:c.7117A>T XP_016865458.1:p.Ile2373Leu
XM_017009970.2:c.7117A>T XP_016865459.1:p.Ile2373Leu
XM_017009971.2:c.7117A>T XP_016865460.1:p.Ile2373Leu
XM_017009972.1:c.235A>T XP_016865461.1:p.Ile79Leu
XM_017009973.1:c.235A>T XP_016865462.1:p.Ile79Leu
XM_017009974.2:c.7117A>T XP_016865463.1:p.Ile2373Leu
NR_003149.2:n.7133A>T