Canonical Allele Identifier: CA360429955
Community Standard Title: NM_032119.4(ADGRV1):c.17258G>A (p.Trp5753Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90853337G>A , CM000667.2:g.90853337G>A GRCh38
NC_000005.9:g.90149154G>A , CM000667.1:g.90149154G>A GRCh37
NC_000005.8:g.90184910G>A NCBI36
NG_007083.1:g.299538G>A
NG_007083.2:g.328994G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17258G>A MANE Select NP_115495.3:p.Trp5753Ter
ENST00000405460.9:c.17258G>A MANE Select ENSP00000384582.2:p.Trp5753Ter
NM_032119.3:c.17258G>A NP_115495.3:p.Trp5753Ter
NR_003149.1:n.17271G>A
NR_003149.2:n.17274G>A
ENST00000405460.6:c.17258G>A ENSP00000384582.2:p.Trp5753Ter
ENST00000425867.2:c.4241G>A ENSP00000392618.2:p.Trp1414Ter
ENST00000425867.3:c.6212G>A ENSP00000392618.3:p.Trp2071Ter
ENST00000505845.2:n.449G>A
ENST00000638510.1:n.4525G>A
ENST00000638990.1:c.470G>A
ENST00000639431.1:c.266-132007G>A ENSP00000491057.1:n.266-132007G>A
ENST00000640407.1:c.3707G>A ENSP00000491425.1:n.3707G>A
XM_011543675.1:c.17255G>A XP_011541977.1:p.Trp5752Ter
XM_011543676.1:c.17177G>A XP_011541978.1:p.Trp5726Ter
XM_011543677.1:c.14561G>A XP_011541979.1:p.Trp4854Ter
XM_017009963.2:c.17279G>A XP_016865452.1:p.Trp5760Ter
XM_017009964.2:c.17276G>A XP_016865453.1:p.Trp5759Ter
XM_017009965.1:c.17276G>A XP_016865454.1:p.Trp5759Ter
XM_017009966.2:c.17198G>A XP_016865455.1:p.Trp5733Ter
XM_017009967.1:c.17183G>A XP_016865456.1:p.Trp5728Ter
XM_017009968.2:c.17099G>A XP_016865457.1:p.Trp5700Ter
XM_017009969.2:c.17279G>A XP_016865458.1:p.Trp5760Ter
XM_017009972.1:c.10397G>A XP_016865461.1:p.Trp3466Ter
XM_017009973.1:c.10376G>A XP_016865462.1:p.Trp3459Ter