Canonical Allele Identifier: CA360397596
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716662C>A , CM000667.2:g.90716662C>A GRCh38
NC_000005.9:g.90012479C>A , CM000667.1:g.90012479C>A GRCh37
NC_000005.8:g.90048235C>A NCBI36
NG_007083.1:g.162863C>A
NG_007083.2:g.192319C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.9380C>A MANE Select ENSP00000384582.2:p.Ser3127Ter
ENST00000639431.1:c.265+40453C>A ENSP00000491057.1:n.265+40453C>A
ENST00000639473.1:n.4839C>A
ENST00000640012.1:c.3187C>A
ENST00000640374.1:n.2524C>A
ENST00000640779.1:c.4109C>A
ENST00000405460.6:c.9380C>A ENSP00000384582.2:p.Ser3127Ter
ENST00000509621.1:c.2077C>A
NM_032119.3:c.9380C>A NP_115495.3:p.Ser3127Ter
NR_003149.1:n.9393C>A
XM_011543675.1:c.9377C>A XP_011541977.1:p.Ser3126Ter
XM_011543676.1:c.9299C>A XP_011541978.1:p.Ser3100Ter
XM_011543677.1:c.6683C>A XP_011541979.1:p.Ser2228Ter
XM_011543678.1:c.9380C>A XP_011541980.1:p.Ser3127Ter
XM_011543679.1:c.9380C>A XP_011541981.1:p.Ser3127Ter
XR_948560.1:n.272-853G>T
NM_032119.4:c.9380C>A MANE Select NP_115495.3:p.Ser3127Ter
XM_017009963.2:c.9401C>A XP_016865452.1:p.Ser3134Ter
XM_017009964.2:c.9398C>A XP_016865453.1:p.Ser3133Ter
XM_017009965.1:c.9398C>A XP_016865454.1:p.Ser3133Ter
XM_017009966.2:c.9320C>A XP_016865455.1:p.Ser3107Ter
XM_017009967.1:c.9305C>A XP_016865456.1:p.Ser3102Ter
XM_017009968.2:c.9401C>A XP_016865457.1:p.Ser3134Ter
XM_017009969.2:c.9401C>A XP_016865458.1:p.Ser3134Ter
XM_017009970.2:c.9401C>A XP_016865459.1:p.Ser3134Ter
XM_017009971.2:c.9401C>A XP_016865460.1:p.Ser3134Ter
XM_017009972.1:c.2519C>A XP_016865461.1:p.Ser840Ter
XM_017009973.1:c.2498C>A XP_016865462.1:p.Ser833Ter
XM_017009974.2:c.9401C>A XP_016865463.1:p.Ser3134Ter
XR_001742802.1:n.2523-853G>T
NR_003149.2:n.9396C>A