Canonical Allele Identifier: CA184901
Community Standard Title: NM_032119.4(ADGRV1):c.9291T>G (p.Ser3097Arg)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716573T>G , CM000667.2:g.90716573T>G GRCh38
NC_000005.9:g.90012390T>G , CM000667.1:g.90012390T>G GRCh37
NC_000005.8:g.90048146T>G NCBI36
NG_007083.1:g.162774T>G
NG_007083.2:g.192230T>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.9291T>G MANE Select NP_115495.3:p.Ser3097Arg
ENST00000405460.9:c.9291T>G MANE Select ENSP00000384582.2:p.Ser3097Arg
NM_032119.3:c.9291T>G NP_115495.3:p.Ser3097Arg
NR_003149.1:n.9304T>G
NR_003149.2:n.9307T>G
ENST00000405460.6:c.9291T>G ENSP00000384582.2:p.Ser3097Arg
ENST00000509621.1:c.1988T>G
ENST00000639431.1:c.265+40364T>G ENSP00000491057.1:n.265+40364T>G
ENST00000639473.1:n.4750T>G
ENST00000640012.1:c.3098T>G
ENST00000640374.1:n.2435T>G
ENST00000640779.1:c.4020T>G
XM_011543675.1:c.9288T>G XP_011541977.1:p.Ser3096Arg
XM_011543676.1:c.9210T>G XP_011541978.1:p.Ser3070Arg
XM_011543677.1:c.6594T>G XP_011541979.1:p.Ser2198Arg
XM_011543678.1:c.9291T>G XP_011541980.1:p.Ser3097Arg
XM_011543679.1:c.9291T>G XP_011541981.1:p.Ser3097Arg
XM_017009963.2:c.9312T>G XP_016865452.1:p.Ser3104Arg
XM_017009964.2:c.9309T>G XP_016865453.1:p.Ser3103Arg
XM_017009965.1:c.9309T>G XP_016865454.1:p.Ser3103Arg
XM_017009966.2:c.9231T>G XP_016865455.1:p.Ser3077Arg
XM_017009967.1:c.9216T>G XP_016865456.1:p.Ser3072Arg
XM_017009968.2:c.9312T>G XP_016865457.1:p.Ser3104Arg
XM_017009969.2:c.9312T>G XP_016865458.1:p.Ser3104Arg
XM_017009970.2:c.9312T>G XP_016865459.1:p.Ser3104Arg
XM_017009971.2:c.9312T>G XP_016865460.1:p.Ser3104Arg
XM_017009972.1:c.2430T>G XP_016865461.1:p.Ser810Arg
XM_017009973.1:c.2409T>G XP_016865462.1:p.Ser803Arg
XM_017009974.2:c.9312T>G XP_016865463.1:p.Ser3104Arg
XR_001742802.1:n.2523-764A>C
XR_948560.1:n.272-764A>C