Canonical Allele Identifier: CA3341548
Community Standard Title: NM_032119.4(ADGRV1):c.13544G>A (p.Gly4515Glu)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90783948G>A , CM000667.2:g.90783948G>A GRCh38
NC_000005.9:g.90079765G>A , CM000667.1:g.90079765G>A GRCh37
NC_000005.8:g.90115521G>A NCBI36
NG_007083.1:g.230149G>A
NG_007083.2:g.259605G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.13544G>A MANE Select NP_115495.3:p.Gly4515Glu
ENST00000405460.9:c.13544G>A MANE Select ENSP00000384582.2:p.Gly4515Glu
NM_032119.3:c.13544G>A NP_115495.3:p.Gly4515Glu
NR_003149.1:n.13557G>A
NR_003149.2:n.13560G>A
ENST00000405460.6:c.13544G>A ENSP00000384582.2:p.Gly4515Glu
ENST00000425867.2:c.527G>A ENSP00000392618.2:p.Gly176Glu
ENST00000425867.3:c.2498G>A ENSP00000392618.3:p.Gly833Glu
ENST00000638510.1:n.811G>A
ENST00000638975.1:c.173G>A ENSP00000492630.1:p.Gly58Glu
ENST00000639431.1:c.265+107739G>A ENSP00000491057.1:n.265+107739G>A
XM_011543675.1:c.13541G>A XP_011541977.1:p.Gly4514Glu
XM_011543676.1:c.13463G>A XP_011541978.1:p.Gly4488Glu
XM_011543677.1:c.10847G>A XP_011541979.1:p.Gly3616Glu
XM_011543678.1:c.13544G>A XP_011541980.1:p.Gly4515Glu
XM_017009963.2:c.13565G>A XP_016865452.1:p.Gly4522Glu
XM_017009964.2:c.13562G>A XP_016865453.1:p.Gly4521Glu
XM_017009965.1:c.13562G>A XP_016865454.1:p.Gly4521Glu
XM_017009966.2:c.13484G>A XP_016865455.1:p.Gly4495Glu
XM_017009967.1:c.13469G>A XP_016865456.1:p.Gly4490Glu
XM_017009968.2:c.13565G>A XP_016865457.1:p.Gly4522Glu
XM_017009969.2:c.13565G>A XP_016865458.1:p.Gly4522Glu
XM_017009970.2:c.13565G>A XP_016865459.1:p.Gly4522Glu
XM_017009971.2:c.13565G>A XP_016865460.1:p.Gly4522Glu
XM_017009972.1:c.6683G>A XP_016865461.1:p.Gly2228Glu
XM_017009973.1:c.6662G>A XP_016865462.1:p.Gly2221Glu