Canonical Allele Identifier: CA360397591
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716661T>G , CM000667.2:g.90716661T>G GRCh38
NC_000005.9:g.90012478T>G , CM000667.1:g.90012478T>G GRCh37
NC_000005.8:g.90048234T>G NCBI36
NG_007083.1:g.162862T>G
NG_007083.2:g.192318T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9379T>G MANE Select ENSP00000384582.2:p.Ser3127Ala
ENST00000639431.1:c.265+40452T>G ENSP00000491057.1:n.265+40452T>G
ENST00000639473.1:n.4838T>G
ENST00000640012.1:c.3186T>G
ENST00000640374.1:n.2523T>G
ENST00000640779.1:c.4108T>G
ENST00000405460.6:c.9379T>G ENSP00000384582.2:p.Ser3127Ala
ENST00000509621.1:c.2076T>G
NM_032119.3:c.9379T>G NP_115495.3:p.Ser3127Ala
NR_003149.1:n.9392T>G
XM_011543675.1:c.9376T>G XP_011541977.1:p.Ser3126Ala
XM_011543676.1:c.9298T>G XP_011541978.1:p.Ser3100Ala
XM_011543677.1:c.6682T>G XP_011541979.1:p.Ser2228Ala
XM_011543678.1:c.9379T>G XP_011541980.1:p.Ser3127Ala
XM_011543679.1:c.9379T>G XP_011541981.1:p.Ser3127Ala
XR_948560.1:n.272-852A>C
NM_032119.4:c.9379T>G MANE Select NP_115495.3:p.Ser3127Ala
XM_017009963.2:c.9400T>G XP_016865452.1:p.Ser3134Ala
XM_017009964.2:c.9397T>G XP_016865453.1:p.Ser3133Ala
XM_017009965.1:c.9397T>G XP_016865454.1:p.Ser3133Ala
XM_017009966.2:c.9319T>G XP_016865455.1:p.Ser3107Ala
XM_017009967.1:c.9304T>G XP_016865456.1:p.Ser3102Ala
XM_017009968.2:c.9400T>G XP_016865457.1:p.Ser3134Ala
XM_017009969.2:c.9400T>G XP_016865458.1:p.Ser3134Ala
XM_017009970.2:c.9400T>G XP_016865459.1:p.Ser3134Ala
XM_017009971.2:c.9400T>G XP_016865460.1:p.Ser3134Ala
XM_017009972.1:c.2518T>G XP_016865461.1:p.Ser840Ala
XM_017009973.1:c.2497T>G XP_016865462.1:p.Ser833Ala
XM_017009974.2:c.9400T>G XP_016865463.1:p.Ser3134Ala
XR_001742802.1:n.2523-852A>C
NR_003149.2:n.9395T>G