Canonical Allele Identifier: CA360376065
Community Standard Title: NM_032119.4(ADGRV1):c.7307T>G (p.Leu2436Arg)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90694063T>G , CM000667.2:g.90694063T>G GRCh38
NC_000005.9:g.89989880T>G , CM000667.1:g.89989880T>G GRCh37
NC_000005.8:g.90025636T>G NCBI36
NG_007083.1:g.140264T>G
NG_007083.2:g.169720T>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.7307T>G MANE Select NP_115495.3:p.Leu2436Arg
ENST00000405460.9:c.7307T>G MANE Select ENSP00000384582.2:p.Leu2436Arg
NM_032119.3:c.7307T>G NP_115495.3:p.Leu2436Arg
NR_003149.1:n.7320T>G
NR_003149.2:n.7323T>G
ENST00000405460.6:c.7307T>G ENSP00000384582.2:p.Leu2436Arg
ENST00000509621.1:c.4T>G
ENST00000639431.1:c.265+17854T>G ENSP00000491057.1:n.265+17854T>G
ENST00000639473.1:n.2766T>G
ENST00000640012.1:c.1114T>G
ENST00000640374.1:n.451T>G
ENST00000640403.1:c.4598T>G ENSP00000492531.1:p.Leu1533Arg
ENST00000640779.1:c.2036T>G
XM_011543675.1:c.7304T>G XP_011541977.1:p.Leu2435Arg
XM_011543676.1:c.7226T>G XP_011541978.1:p.Leu2409Arg
XM_011543677.1:c.4610T>G XP_011541979.1:p.Leu1537Arg
XM_011543678.1:c.7307T>G XP_011541980.1:p.Leu2436Arg
XM_011543679.1:c.7307T>G XP_011541981.1:p.Leu2436Arg
XM_017009963.2:c.7307T>G XP_016865452.1:p.Leu2436Arg
XM_017009964.2:c.7304T>G XP_016865453.1:p.Leu2435Arg
XM_017009965.1:c.7304T>G XP_016865454.1:p.Leu2435Arg
XM_017009966.2:c.7226T>G XP_016865455.1:p.Leu2409Arg
XM_017009967.1:c.7211T>G XP_016865456.1:p.Leu2404Arg
XM_017009968.2:c.7307T>G XP_016865457.1:p.Leu2436Arg
XM_017009969.2:c.7307T>G XP_016865458.1:p.Leu2436Arg
XM_017009970.2:c.7307T>G XP_016865459.1:p.Leu2436Arg
XM_017009971.2:c.7307T>G XP_016865460.1:p.Leu2436Arg
XM_017009972.1:c.425T>G XP_016865461.1:p.Leu142Arg
XM_017009973.1:c.425T>G XP_016865462.1:p.Leu142Arg
XM_017009974.2:c.7307T>G XP_016865463.1:p.Leu2436Arg