Canonical Allele Identifier: CA360367193
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755149C>G , CM000667.2:g.90755149C>G GRCh38
NC_000005.9:g.90050966C>G , CM000667.1:g.90050966C>G GRCh37
NC_000005.8:g.90086722C>G NCBI36
NG_007083.1:g.201350C>G
NG_007083.2:g.230806C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11544C>G MANE Select ENSP00000384582.2:p.Asn3848Lys
ENST00000425867.3:c.675C>G ENSP00000392618.3:p.Asn225Lys
ENST00000639431.1:c.265+78940C>G ENSP00000491057.1:n.265+78940C>G
ENST00000640374.1:n.4688C>G
ENST00000640464.1:n.1963C>G
ENST00000405460.6:c.11544C>G ENSP00000384582.2:p.Asn3848Lys
ENST00000509621.1:c.4241C>G
NM_032119.3:c.11544C>G NP_115495.3:p.Asn3848Lys
NR_003149.1:n.11557C>G
XM_011543675.1:c.11541C>G XP_011541977.1:p.Asn3847Lys
XM_011543676.1:c.11463C>G XP_011541978.1:p.Asn3821Lys
XM_011543677.1:c.8847C>G XP_011541979.1:p.Asn2949Lys
XM_011543678.1:c.11544C>G XP_011541980.1:p.Asn3848Lys
NM_032119.4:c.11544C>G MANE Select NP_115495.3:p.Asn3848Lys
XM_017009963.2:c.11565C>G XP_016865452.1:p.Asn3855Lys
XM_017009964.2:c.11562C>G XP_016865453.1:p.Asn3854Lys
XM_017009965.1:c.11562C>G XP_016865454.1:p.Asn3854Lys
XM_017009966.2:c.11484C>G XP_016865455.1:p.Asn3828Lys
XM_017009967.1:c.11469C>G XP_016865456.1:p.Asn3823Lys
XM_017009968.2:c.11565C>G XP_016865457.1:p.Asn3855Lys
XM_017009969.2:c.11565C>G XP_016865458.1:p.Asn3855Lys
XM_017009970.2:c.11565C>G XP_016865459.1:p.Asn3855Lys
XM_017009971.2:c.11565C>G XP_016865460.1:p.Asn3855Lys
XM_017009972.1:c.4683C>G XP_016865461.1:p.Asn1561Lys
XM_017009973.1:c.4662C>G XP_016865462.1:p.Asn1554Lys
NR_003149.2:n.11560C>G