Canonical Allele Identifier: CA360431273
Community Standard Title: NM_032119.4(ADGRV1):c.18330T>A (p.Tyr6110Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.91102238T>A , CM000667.2:g.91102238T>A GRCh38
NC_000005.9:g.90398055T>A , CM000667.1:g.90398055T>A GRCh37
NC_000005.8:g.90433811T>A NCBI36
NG_007083.1:g.548439T>A
NG_007083.2:g.577895T>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.18330T>A MANE Select NP_115495.3:p.Tyr6110Ter
ENST00000405460.9:c.18330T>A MANE Select ENSP00000384582.2:p.Tyr6110Ter
NM_032119.3:c.18330T>A NP_115495.3:p.Tyr6110Ter
NR_003149.1:n.18343T>A
NR_003149.2:n.18346T>A
ENST00000405460.6:c.18330T>A ENSP00000384582.2:p.Tyr6110Ter
ENST00000425867.2:c.5313T>A ENSP00000392618.2:p.Tyr1771Ter
ENST00000425867.3:c.7284T>A ENSP00000392618.3:p.Tyr2428Ter
ENST00000638510.1:n.5597T>A
ENST00000638990.1:c.1542T>A
ENST00000639212.1:n.250T>A
ENST00000639530.1:n.198T>A
ENST00000639821.1:c.414T>A ENSP00000492216.1:p.Tyr138Ter
ENST00000640256.1:n.198T>A
ENST00000640407.1:c.4779T>A ENSP00000491425.1:n.4779T>A
ENST00000640815.1:c.414T>A ENSP00000491767.1:p.Tyr138Ter
XM_011543675.1:c.18327T>A XP_011541977.1:p.Tyr6109Ter
XM_011543676.1:c.18249T>A XP_011541978.1:p.Tyr6083Ter
XM_011543677.1:c.15633T>A XP_011541979.1:p.Tyr5211Ter
XM_017009963.2:c.18351T>A XP_016865452.1:p.Tyr6117Ter
XM_017009964.2:c.18348T>A XP_016865453.1:p.Tyr6116Ter
XM_017009965.1:c.18348T>A XP_016865454.1:p.Tyr6116Ter
XM_017009966.2:c.18270T>A XP_016865455.1:p.Tyr6090Ter
XM_017009967.1:c.18255T>A XP_016865456.1:p.Tyr6085Ter
XM_017009968.2:c.18171T>A XP_016865457.1:p.Tyr6057Ter
XM_017009969.2:c.18351T>A XP_016865458.1:p.Tyr6117Ter
XM_017009972.1:c.11469T>A XP_016865461.1:p.Tyr3823Ter
XM_017009973.1:c.11448T>A XP_016865462.1:p.Tyr3816Ter