Canonical Allele Identifier: CA360429067
Community Standard Title: NM_032119.4(ADGRV1):c.17988G>A (p.Trp5996Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90985358G>A , CM000667.2:g.90985358G>A GRCh38
NC_000005.9:g.90281175G>A , CM000667.1:g.90281175G>A GRCh37
NC_000005.8:g.90316931G>A NCBI36
NG_007083.1:g.431559G>A
NG_007083.2:g.461015G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17988G>A MANE Select NP_115495.3:p.Trp5996Ter
ENST00000405460.9:c.17988G>A MANE Select ENSP00000384582.2:p.Trp5996Ter
NM_032119.3:c.17988G>A NP_115495.3:p.Trp5996Ter
NR_003149.1:n.18001G>A
NR_003149.2:n.18004G>A
ENST00000405460.6:c.17988G>A ENSP00000384582.2:p.Trp5996Ter
ENST00000425867.2:c.4971G>A ENSP00000392618.2:p.Trp1657Ter
ENST00000425867.3:c.6942G>A ENSP00000392618.3:p.Trp2314Ter
ENST00000638510.1:n.5255G>A
ENST00000638990.1:c.1200G>A
ENST00000639431.1:c.280G>A ENSP00000491057.1:p.Val94Ile
ENST00000639707.1:c.72G>A ENSP00000492328.1:p.Trp24Ter
ENST00000639821.1:c.72G>A ENSP00000492216.1:p.Trp24Ter
ENST00000640369.1:c.72G>A ENSP00000491401.1:p.Trp24Ter
ENST00000640407.1:c.4437G>A ENSP00000491425.1:n.4437G>A
ENST00000640815.1:c.72G>A ENSP00000491767.1:p.Trp24Ter
XM_011543675.1:c.17985G>A XP_011541977.1:p.Trp5995Ter
XM_011543676.1:c.17907G>A XP_011541978.1:p.Trp5969Ter
XM_011543677.1:c.15291G>A XP_011541979.1:p.Trp5097Ter
XM_017009963.2:c.18009G>A XP_016865452.1:p.Trp6003Ter
XM_017009964.2:c.18006G>A XP_016865453.1:p.Trp6002Ter
XM_017009965.1:c.18006G>A XP_016865454.1:p.Trp6002Ter
XM_017009966.2:c.17928G>A XP_016865455.1:p.Trp5976Ter
XM_017009967.1:c.17913G>A XP_016865456.1:p.Trp5971Ter
XM_017009968.2:c.17829G>A XP_016865457.1:p.Trp5943Ter
XM_017009969.2:c.18009G>A XP_016865458.1:p.Trp6003Ter
XM_017009972.1:c.11127G>A XP_016865461.1:p.Trp3709Ter
XM_017009973.1:c.11106G>A XP_016865462.1:p.Trp3702Ter