Canonical Allele Identifier: CA360371566
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692720A>T , CM000667.2:g.90692720A>T GRCh38
NC_000005.9:g.89988537A>T , CM000667.1:g.89988537A>T GRCh37
NC_000005.8:g.90024293A>T NCBI36
NG_007083.1:g.138921A>T
NG_007083.2:g.168377A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7067A>T MANE Select ENSP00000384582.2:p.Gln2356Leu
ENST00000639431.1:c.265+16511A>T ENSP00000491057.1:n.265+16511A>T
ENST00000639473.1:n.2526A>T
ENST00000640012.1:c.874A>T
ENST00000640374.1:n.211A>T
ENST00000640403.1:c.4358A>T ENSP00000492531.1:p.Gln1453Leu
ENST00000640779.1:c.1796A>T
ENST00000405460.6:c.7067A>T ENSP00000384582.2:p.Gln2356Leu
NM_032119.3:c.7067A>T NP_115495.3:p.Gln2356Leu
NR_003149.1:n.7080A>T
XM_011543675.1:c.7064A>T XP_011541977.1:p.Gln2355Leu
XM_011543676.1:c.6986A>T XP_011541978.1:p.Gln2329Leu
XM_011543677.1:c.4370A>T XP_011541979.1:p.Gln1457Leu
XM_011543678.1:c.7067A>T XP_011541980.1:p.Gln2356Leu
XM_011543679.1:c.7067A>T XP_011541981.1:p.Gln2356Leu
NM_032119.4:c.7067A>T MANE Select NP_115495.3:p.Gln2356Leu
XM_017009963.2:c.7067A>T XP_016865452.1:p.Gln2356Leu
XM_017009964.2:c.7064A>T XP_016865453.1:p.Gln2355Leu
XM_017009965.1:c.7064A>T XP_016865454.1:p.Gln2355Leu
XM_017009966.2:c.6986A>T XP_016865455.1:p.Gln2329Leu
XM_017009967.1:c.6971A>T XP_016865456.1:p.Gln2324Leu
XM_017009968.2:c.7067A>T XP_016865457.1:p.Gln2356Leu
XM_017009969.2:c.7067A>T XP_016865458.1:p.Gln2356Leu
XM_017009970.2:c.7067A>T XP_016865459.1:p.Gln2356Leu
XM_017009971.2:c.7067A>T XP_016865460.1:p.Gln2356Leu
XM_017009972.1:c.185A>T XP_016865461.1:p.Gln62Leu
XM_017009973.1:c.185A>T XP_016865462.1:p.Gln62Leu
XM_017009974.2:c.7067A>T XP_016865463.1:p.Gln2356Leu
NR_003149.2:n.7083A>T