Canonical Allele Identifier: CA645559071
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692695_90692696delinsTT , CM000667.2:g.90692695_90692696delinsTT GRCh38
NC_000005.9:g.89988512_89988513delinsTT , CM000667.1:g.89988512_89988513delinsTT GRCh37
NC_000005.8:g.90024268_90024269delinsTT NCBI36
NG_007083.1:g.138896_138897delinsTT
NG_007083.2:g.168352_168353delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7042_7043delinsTT MANE Select ENSP00000384582.2:p.Pro2348Phe
ENST00000639431.1:c.265+16486_265+16487delinsTT ENSP00000491057.1:n.265+16486_265+16487delinsTT
ENST00000639473.1:n.2501_2502delinsTT
ENST00000640012.1:c.849_850delinsTT
ENST00000640374.1:n.186_187delinsTT
ENST00000640403.1:c.4333_4334delinsTT ENSP00000492531.1:p.Pro1445Phe
ENST00000640779.1:c.1771_1772delinsTT
ENST00000405460.6:c.7042_7043delinsTT ENSP00000384582.2:p.Pro2348Phe
NM_032119.3:c.7042_7043delinsTT NP_115495.3:p.Pro2348Phe
NR_003149.1:n.7055_7056delinsTT
XM_011543675.1:c.7039_7040delinsTT XP_011541977.1:p.Pro2347Phe
XM_011543676.1:c.6961_6962delinsTT XP_011541978.1:p.Pro2321Phe
XM_011543677.1:c.4345_4346delinsTT XP_011541979.1:p.Pro1449Phe
XM_011543678.1:c.7042_7043delinsTT XP_011541980.1:p.Pro2348Phe
XM_011543679.1:c.7042_7043delinsTT XP_011541981.1:p.Pro2348Phe
NM_032119.4:c.7042_7043delinsTT MANE Select NP_115495.3:p.Pro2348Phe
XM_017009963.2:c.7042_7043delinsTT XP_016865452.1:p.Pro2348Phe
XM_017009964.2:c.7039_7040delinsTT XP_016865453.1:p.Pro2347Phe
XM_017009965.1:c.7039_7040delinsTT XP_016865454.1:p.Pro2347Phe
XM_017009966.2:c.6961_6962delinsTT XP_016865455.1:p.Pro2321Phe
XM_017009967.1:c.6946_6947delinsTT XP_016865456.1:p.Pro2316Phe
XM_017009968.2:c.7042_7043delinsTT XP_016865457.1:p.Pro2348Phe
XM_017009969.2:c.7042_7043delinsTT XP_016865458.1:p.Pro2348Phe
XM_017009970.2:c.7042_7043delinsTT XP_016865459.1:p.Pro2348Phe
XM_017009971.2:c.7042_7043delinsTT XP_016865460.1:p.Pro2348Phe
XM_017009972.1:c.160_161delinsTT XP_016865461.1:p.Pro54Phe
XM_017009973.1:c.160_161delinsTT XP_016865462.1:p.Pro54Phe
XM_017009974.2:c.7042_7043delinsTT XP_016865463.1:p.Pro2348Phe
NR_003149.2:n.7058_7059delinsTT