Canonical Allele Identifier: CA360425493
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823449T>G , CM000667.2:g.90823449T>G GRCh38
NC_000005.9:g.90119266T>G , CM000667.1:g.90119266T>G GRCh37
NC_000005.8:g.90155022T>G NCBI36
NG_007083.1:g.269650T>G
NG_007083.2:g.299106T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16221T>G MANE Select ENSP00000384582.2:p.Phe5407Leu
ENST00000425867.3:c.5175T>G ENSP00000392618.3:p.Phe1725Leu
ENST00000638510.1:n.3488T>G
ENST00000639431.1:c.265+147240T>G ENSP00000491057.1:n.265+147240T>G
ENST00000640061.1:n.128+1267T>G
ENST00000640407.1:c.2631T>G ENSP00000491425.1:p.Phe877Leu
ENST00000405460.6:c.16221T>G ENSP00000384582.2:p.Phe5407Leu
ENST00000425867.2:c.3204T>G ENSP00000392618.2:p.Phe1068Leu
NM_032119.3:c.16221T>G NP_115495.3:p.Phe5407Leu
NR_003149.1:n.16234T>G
XM_011543675.1:c.16218T>G XP_011541977.1:p.Phe5406Leu
XM_011543676.1:c.16140T>G XP_011541978.1:p.Phe5380Leu
XM_011543677.1:c.13524T>G XP_011541979.1:p.Phe4508Leu
NM_032119.4:c.16221T>G MANE Select NP_115495.3:p.Phe5407Leu
XM_017009963.2:c.16242T>G XP_016865452.1:p.Phe5414Leu
XM_017009964.2:c.16239T>G XP_016865453.1:p.Phe5413Leu
XM_017009965.1:c.16239T>G XP_016865454.1:p.Phe5413Leu
XM_017009966.2:c.16161T>G XP_016865455.1:p.Phe5387Leu
XM_017009967.1:c.16146T>G XP_016865456.1:p.Phe5382Leu
XM_017009968.2:c.16062T>G XP_016865457.1:p.Phe5354Leu
XM_017009969.2:c.16242T>G XP_016865458.1:p.Phe5414Leu
XM_017009972.1:c.9360T>G XP_016865461.1:p.Phe3120Leu
XM_017009973.1:c.9339T>G XP_016865462.1:p.Phe3113Leu
NR_003149.2:n.16237T>G