Canonical Allele Identifier: CA3340051
Community Standard Title: NM_032119.4(ADGRV1):c.7540C>G (p.Gln2514Glu)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90694296C>G , CM000667.2:g.90694296C>G GRCh38
NC_000005.9:g.89990113C>G , CM000667.1:g.89990113C>G GRCh37
NC_000005.8:g.90025869C>G NCBI36
NG_007083.1:g.140497C>G
NG_007083.2:g.169953C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.7540C>G MANE Select NP_115495.3:p.Gln2514Glu
ENST00000405460.9:c.7540C>G MANE Select ENSP00000384582.2:p.Gln2514Glu
NM_032119.3:c.7540C>G NP_115495.3:p.Gln2514Glu
NR_003149.1:n.7553C>G
NR_003149.2:n.7556C>G
ENST00000405460.6:c.7540C>G ENSP00000384582.2:p.Gln2514Glu
ENST00000509621.1:c.237C>G
ENST00000639431.1:c.265+18087C>G ENSP00000491057.1:n.265+18087C>G
ENST00000639473.1:n.2999C>G
ENST00000640012.1:c.1347C>G
ENST00000640374.1:n.684C>G
ENST00000640403.1:c.4831C>G ENSP00000492531.1:p.Gln1611Glu
ENST00000640779.1:c.2269C>G
XM_011543675.1:c.7537C>G XP_011541977.1:p.Gln2513Glu
XM_011543676.1:c.7459C>G XP_011541978.1:p.Gln2487Glu
XM_011543677.1:c.4843C>G XP_011541979.1:p.Gln1615Glu
XM_011543678.1:c.7540C>G XP_011541980.1:p.Gln2514Glu
XM_011543679.1:c.7540C>G XP_011541981.1:p.Gln2514Glu
XM_017009963.2:c.7540C>G XP_016865452.1:p.Gln2514Glu
XM_017009964.2:c.7537C>G XP_016865453.1:p.Gln2513Glu
XM_017009965.1:c.7537C>G XP_016865454.1:p.Gln2513Glu
XM_017009966.2:c.7459C>G XP_016865455.1:p.Gln2487Glu
XM_017009967.1:c.7444C>G XP_016865456.1:p.Gln2482Glu
XM_017009968.2:c.7540C>G XP_016865457.1:p.Gln2514Glu
XM_017009969.2:c.7540C>G XP_016865458.1:p.Gln2514Glu
XM_017009970.2:c.7540C>G XP_016865459.1:p.Gln2514Glu
XM_017009971.2:c.7540C>G XP_016865460.1:p.Gln2514Glu
XM_017009972.1:c.658C>G XP_016865461.1:p.Gln220Glu
XM_017009973.1:c.658C>G XP_016865462.1:p.Gln220Glu
XM_017009974.2:c.7540C>G XP_016865463.1:p.Gln2514Glu