Canonical Allele Identifier: CA360366214
Community Standard Title: NM_032119.4(ADGRV1):c.6564T>G (p.Tyr2188Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90689934T>G , CM000667.2:g.90689934T>G GRCh38
NC_000005.9:g.89985751T>G , CM000667.1:g.89985751T>G GRCh37
NC_000005.8:g.90021507T>G NCBI36
NG_007083.1:g.136135T>G
NG_007083.2:g.165591T>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.6564T>G MANE Select NP_115495.3:p.Tyr2188Ter
ENST00000405460.9:c.6564T>G MANE Select ENSP00000384582.2:p.Tyr2188Ter
NM_032119.3:c.6564T>G NP_115495.3:p.Tyr2188Ter
NR_003149.1:n.6660T>G
NR_003149.2:n.6663T>G
ENST00000405460.6:c.6564T>G ENSP00000384582.2:p.Tyr2188Ter
ENST00000639431.1:c.265+13725T>G ENSP00000491057.1:n.265+13725T>G
ENST00000639473.1:n.2023T>G
ENST00000640012.1:c.454T>G
ENST00000640403.1:c.3855T>G ENSP00000492531.1:p.Tyr1285Ter
ENST00000640779.1:c.1376T>G
XM_011543675.1:c.6561T>G XP_011541977.1:p.Tyr2187Ter
XM_011543676.1:c.6483T>G XP_011541978.1:p.Tyr2161Ter
XM_011543677.1:c.3867T>G XP_011541979.1:p.Tyr1289Ter
XM_011543678.1:c.6564T>G XP_011541980.1:p.Tyr2188Ter
XM_011543679.1:c.6564T>G XP_011541981.1:p.Tyr2188Ter
XM_017009963.2:c.6564T>G XP_016865452.1:p.Tyr2188Ter
XM_017009964.2:c.6561T>G XP_016865453.1:p.Tyr2187Ter
XM_017009965.1:c.6561T>G XP_016865454.1:p.Tyr2187Ter
XM_017009966.2:c.6483T>G XP_016865455.1:p.Tyr2161Ter
XM_017009967.1:c.6468T>G XP_016865456.1:p.Tyr2156Ter
XM_017009968.2:c.6564T>G XP_016865457.1:p.Tyr2188Ter
XM_017009969.2:c.6564T>G XP_016865458.1:p.Tyr2188Ter
XM_017009970.2:c.6564T>G XP_016865459.1:p.Tyr2188Ter
XM_017009971.2:c.6564T>G XP_016865460.1:p.Tyr2188Ter
XM_017009972.1:c.-236T>G XP_016865461.1:n.-236T>G
XM_017009973.1:c.-236T>G XP_016865462.1:n.-236T>G
XM_017009974.2:c.6564T>G XP_016865463.1:p.Tyr2188Ter