Canonical Allele Identifier: CA360414037
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90683980A>C , CM000667.2:g.90683980A>C GRCh38
NC_000005.9:g.89979797A>C , CM000667.1:g.89979797A>C GRCh37
NC_000005.8:g.90015553A>C NCBI36
NG_007083.1:g.130181A>C
NG_007083.2:g.159637A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.6059A>C MANE Select ENSP00000384582.2:p.Asp2020Ala
ENST00000639431.1:c.265+7771A>C ENSP00000491057.1:n.265+7771A>C
ENST00000639473.1:n.1518A>C
ENST00000640012.1:c.165-1800A>C
ENST00000640403.1:c.3350A>C ENSP00000492531.1:p.Asp1117Ala
ENST00000640779.1:c.871A>C
ENST00000405460.6:c.6059A>C ENSP00000384582.2:p.Asp2020Ala
NM_032119.3:c.6059A>C NP_115495.3:p.Asp2020Ala
NR_003149.1:n.6155A>C
XM_011543675.1:c.6056A>C XP_011541977.1:p.Asp2019Ala
XM_011543676.1:c.5978A>C XP_011541978.1:p.Asp1993Ala
XM_011543677.1:c.3362A>C XP_011541979.1:p.Asp1121Ala
XM_011543678.1:c.6059A>C XP_011541980.1:p.Asp2020Ala
XM_011543679.1:c.6059A>C XP_011541981.1:p.Asp2020Ala
NM_032119.4:c.6059A>C MANE Select NP_115495.3:p.Asp2020Ala
XM_017009963.2:c.6059A>C XP_016865452.1:p.Asp2020Ala
XM_017009964.2:c.6056A>C XP_016865453.1:p.Asp2019Ala
XM_017009965.1:c.6056A>C XP_016865454.1:p.Asp2019Ala
XM_017009966.2:c.5978A>C XP_016865455.1:p.Asp1993Ala
XM_017009967.1:c.5963A>C XP_016865456.1:p.Asp1988Ala
XM_017009968.2:c.6059A>C XP_016865457.1:p.Asp2020Ala
XM_017009969.2:c.6059A>C XP_016865458.1:p.Asp2020Ala
XM_017009970.2:c.6059A>C XP_016865459.1:p.Asp2020Ala
XM_017009971.2:c.6059A>C XP_016865460.1:p.Asp2020Ala
XM_017009973.1:c.-741A>C XP_016865462.1:n.-741A>C
XM_017009974.2:c.6059A>C XP_016865463.1:p.Asp2020Ala
NR_003149.2:n.6158A>C