Canonical Allele Identifier: CA360365656
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627290C>G , CM000667.2:g.90627290C>G GRCh38
NC_000005.9:g.89923107C>G , CM000667.1:g.89923107C>G GRCh37
NC_000005.8:g.89958863C>G NCBI36
NG_007083.1:g.73491C>G
NG_007083.2:g.102947C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.752C>G MANE Select ENSP00000384582.2:p.Ser251Cys
ENST00000640083.1:n.457C>G
ENST00000640109.1:n.848C>G
ENST00000640281.1:n.811C>G
ENST00000405460.6:c.752C>G ENSP00000384582.2:p.Ser251Cys
NM_032119.3:c.752C>G NP_115495.3:p.Ser251Cys
NR_003149.1:n.848C>G
XM_011543675.1:c.752C>G XP_011541977.1:p.Ser251Cys
XM_011543676.1:c.752C>G XP_011541978.1:p.Ser251Cys
XM_011543678.1:c.752C>G XP_011541980.1:p.Ser251Cys
XM_011543679.1:c.752C>G XP_011541981.1:p.Ser251Cys
NM_032119.4:c.752C>G MANE Select NP_115495.3:p.Ser251Cys
XM_017009963.2:c.752C>G XP_016865452.1:p.Ser251Cys
XM_017009964.2:c.752C>G XP_016865453.1:p.Ser251Cys
XM_017009965.1:c.749C>G XP_016865454.1:p.Ser250Cys
XM_017009966.2:c.752C>G XP_016865455.1:p.Ser251Cys
XM_017009967.1:c.656C>G XP_016865456.1:p.Ser219Cys
XM_017009968.2:c.752C>G XP_016865457.1:p.Ser251Cys
XM_017009969.2:c.752C>G XP_016865458.1:p.Ser251Cys
XM_017009970.2:c.752C>G XP_016865459.1:p.Ser251Cys
XM_017009971.2:c.752C>G XP_016865460.1:p.Ser251Cys
XM_017009974.2:c.752C>G XP_016865463.1:p.Ser251Cys
NR_003149.2:n.851C>G