Canonical Allele Identifier: CA360429813
Community Standard Title: NM_032119.4(ADGRV1):c.17200G>T (p.Glu5734Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90848817G>T , CM000667.2:g.90848817G>T GRCh38
NC_000005.9:g.90144634G>T , CM000667.1:g.90144634G>T GRCh37
NC_000005.8:g.90180390G>T NCBI36
NG_007083.1:g.295018G>T
NG_007083.2:g.324474G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17200G>T MANE Select NP_115495.3:p.Glu5734Ter
ENST00000405460.9:c.17200G>T MANE Select ENSP00000384582.2:p.Glu5734Ter
NM_032119.3:c.17200G>T NP_115495.3:p.Glu5734Ter
NR_003149.1:n.17213G>T
NR_003149.2:n.17216G>T
ENST00000405460.6:c.17200G>T ENSP00000384582.2:p.Glu5734Ter
ENST00000425867.2:c.4183G>T ENSP00000392618.2:p.Glu1395Ter
ENST00000425867.3:c.6154G>T ENSP00000392618.3:p.Glu2052Ter
ENST00000505845.1:n.391G>T
ENST00000505845.2:n.391G>T
ENST00000638510.1:n.4467G>T
ENST00000638990.1:c.221G>T
ENST00000639431.1:c.266-136527G>T ENSP00000491057.1:n.266-136527G>T
ENST00000640407.1:c.3649G>T ENSP00000491425.1:n.3649G>T
XM_011543675.1:c.17197G>T XP_011541977.1:p.Glu5733Ter
XM_011543676.1:c.17119G>T XP_011541978.1:p.Glu5707Ter
XM_011543677.1:c.14503G>T XP_011541979.1:p.Glu4835Ter
XM_017009963.2:c.17221G>T XP_016865452.1:p.Glu5741Ter
XM_017009964.2:c.17218G>T XP_016865453.1:p.Glu5740Ter
XM_017009965.1:c.17218G>T XP_016865454.1:p.Glu5740Ter
XM_017009966.2:c.17140G>T XP_016865455.1:p.Glu5714Ter
XM_017009967.1:c.17125G>T XP_016865456.1:p.Glu5709Ter
XM_017009968.2:c.17041G>T XP_016865457.1:p.Glu5681Ter
XM_017009969.2:c.17221G>T XP_016865458.1:p.Glu5741Ter
XM_017009972.1:c.10339G>T XP_016865461.1:p.Glu3447Ter
XM_017009973.1:c.10318G>T XP_016865462.1:p.Glu3440Ter