Canonical Allele Identifier: CA3339710
Community Standard Title: NM_032119.4(ADGRV1):c.6116A>G (p.Asp2039Gly)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90684037A>G , CM000667.2:g.90684037A>G GRCh38
NC_000005.9:g.89979854A>G , CM000667.1:g.89979854A>G GRCh37
NC_000005.8:g.90015610A>G NCBI36
NG_007083.1:g.130238A>G
NG_007083.2:g.159694A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.6116A>G MANE Select NP_115495.3:p.Asp2039Gly
ENST00000405460.9:c.6116A>G MANE Select ENSP00000384582.2:p.Asp2039Gly
NM_032119.3:c.6116A>G NP_115495.3:p.Asp2039Gly
NR_003149.1:n.6212A>G
NR_003149.2:n.6215A>G
ENST00000405460.6:c.6116A>G ENSP00000384582.2:p.Asp2039Gly
ENST00000639431.1:c.265+7828A>G ENSP00000491057.1:n.265+7828A>G
ENST00000639473.1:n.1575A>G
ENST00000640012.1:c.165-1743A>G
ENST00000640403.1:c.3407A>G ENSP00000492531.1:p.Asp1136Gly
ENST00000640779.1:c.928A>G
XM_011543675.1:c.6113A>G XP_011541977.1:p.Asp2038Gly
XM_011543676.1:c.6035A>G XP_011541978.1:p.Asp2012Gly
XM_011543677.1:c.3419A>G XP_011541979.1:p.Asp1140Gly
XM_011543678.1:c.6116A>G XP_011541980.1:p.Asp2039Gly
XM_011543679.1:c.6116A>G XP_011541981.1:p.Asp2039Gly
XM_017009963.2:c.6116A>G XP_016865452.1:p.Asp2039Gly
XM_017009964.2:c.6113A>G XP_016865453.1:p.Asp2038Gly
XM_017009965.1:c.6113A>G XP_016865454.1:p.Asp2038Gly
XM_017009966.2:c.6035A>G XP_016865455.1:p.Asp2012Gly
XM_017009967.1:c.6020A>G XP_016865456.1:p.Asp2007Gly
XM_017009968.2:c.6116A>G XP_016865457.1:p.Asp2039Gly
XM_017009969.2:c.6116A>G XP_016865458.1:p.Asp2039Gly
XM_017009970.2:c.6116A>G XP_016865459.1:p.Asp2039Gly
XM_017009971.2:c.6116A>G XP_016865460.1:p.Asp2039Gly
XM_017009973.1:c.-684A>G XP_016865462.1:n.-684A>G
XM_017009974.2:c.6116A>G XP_016865463.1:p.Asp2039Gly