Canonical Allele Identifier: CA360414226
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90684068T>G , CM000667.2:g.90684068T>G GRCh38
NC_000005.9:g.89979885T>G , CM000667.1:g.89979885T>G GRCh37
NC_000005.8:g.90015641T>G NCBI36
NG_007083.1:g.130269T>G
NG_007083.2:g.159725T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.6147T>G MANE Select ENSP00000384582.2:p.Phe2049Leu
ENST00000639431.1:c.265+7859T>G ENSP00000491057.1:n.265+7859T>G
ENST00000639473.1:n.1606T>G
ENST00000640012.1:c.165-1712T>G
ENST00000640403.1:c.3438T>G ENSP00000492531.1:p.Phe1146Leu
ENST00000640779.1:c.959T>G
ENST00000405460.6:c.6147T>G ENSP00000384582.2:p.Phe2049Leu
NM_032119.3:c.6147T>G NP_115495.3:p.Phe2049Leu
NR_003149.1:n.6243T>G
XM_011543675.1:c.6144T>G XP_011541977.1:p.Phe2048Leu
XM_011543676.1:c.6066T>G XP_011541978.1:p.Phe2022Leu
XM_011543677.1:c.3450T>G XP_011541979.1:p.Phe1150Leu
XM_011543678.1:c.6147T>G XP_011541980.1:p.Phe2049Leu
XM_011543679.1:c.6147T>G XP_011541981.1:p.Phe2049Leu
NM_032119.4:c.6147T>G MANE Select NP_115495.3:p.Phe2049Leu
XM_017009963.2:c.6147T>G XP_016865452.1:p.Phe2049Leu
XM_017009964.2:c.6144T>G XP_016865453.1:p.Phe2048Leu
XM_017009965.1:c.6144T>G XP_016865454.1:p.Phe2048Leu
XM_017009966.2:c.6066T>G XP_016865455.1:p.Phe2022Leu
XM_017009967.1:c.6051T>G XP_016865456.1:p.Phe2017Leu
XM_017009968.2:c.6147T>G XP_016865457.1:p.Phe2049Leu
XM_017009969.2:c.6147T>G XP_016865458.1:p.Phe2049Leu
XM_017009970.2:c.6147T>G XP_016865459.1:p.Phe2049Leu
XM_017009971.2:c.6147T>G XP_016865460.1:p.Phe2049Leu
XM_017009973.1:c.-653T>G XP_016865462.1:n.-653T>G
XM_017009974.2:c.6147T>G XP_016865463.1:p.Phe2049Leu
NR_003149.2:n.6246T>G