Canonical Allele Identifier: CA1562859256
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692633_90692634delinsCT , CM000667.2:g.90692633_90692634delinsCT GRCh38
NC_000005.9:g.89988450_89988451delinsCT , CM000667.1:g.89988450_89988451delinsCT GRCh37
NC_000005.8:g.90024206_90024207delinsCT NCBI36
NG_007083.1:g.138834_138835delinsCT
NG_007083.2:g.168290_168291delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.6980_6981delinsCT MANE Select ENSP00000384582.2:p.Ser2327=
ENST00000639431.1:c.265+16424_265+16425delinsCT ENSP00000491057.1:n.265+16424_265+16425de...
ENST00000639473.1:n.2439_2440delinsCT
ENST00000640012.1:c.787_788delinsCT
ENST00000640374.1:n.124_125delinsCT
ENST00000640403.1:c.4271_4272delinsCT ENSP00000492531.1:p.Ser1424=
ENST00000640779.1:c.1709_1710delinsCT
ENST00000405460.6:c.6980_6981delinsCT ENSP00000384582.2:p.Ser2327=
NM_032119.3:c.6980_6981delinsCT NP_115495.3:p.Ser2327=
NR_003149.1:n.6993_6994delinsCT
XM_011543675.1:c.6977_6978delinsCT XP_011541977.1:p.Ser2326=
XM_011543676.1:c.6899_6900delinsCT XP_011541978.1:p.Ser2300=
XM_011543677.1:c.4283_4284delinsCT XP_011541979.1:p.Ser1428=
XM_011543678.1:c.6980_6981delinsCT XP_011541980.1:p.Ser2327=
XM_011543679.1:c.6980_6981delinsCT XP_011541981.1:p.Ser2327=
NM_032119.4:c.6980_6981delinsCT MANE Select NP_115495.3:p.Ser2327=
XM_017009963.2:c.6980_6981delinsCT XP_016865452.1:p.Ser2327=
XM_017009964.2:c.6977_6978delinsCT XP_016865453.1:p.Ser2326=
XM_017009965.1:c.6977_6978delinsCT XP_016865454.1:p.Ser2326=
XM_017009966.2:c.6899_6900delinsCT XP_016865455.1:p.Ser2300=
XM_017009967.1:c.6884_6885delinsCT XP_016865456.1:p.Ser2295=
XM_017009968.2:c.6980_6981delinsCT XP_016865457.1:p.Ser2327=
XM_017009969.2:c.6980_6981delinsCT XP_016865458.1:p.Ser2327=
XM_017009970.2:c.6980_6981delinsCT XP_016865459.1:p.Ser2327=
XM_017009971.2:c.6980_6981delinsCT XP_016865460.1:p.Ser2327=
XM_017009972.1:c.98_99delinsCT XP_016865461.1:p.Ser33=
XM_017009973.1:c.98_99delinsCT XP_016865462.1:p.Ser33=
XM_017009974.2:c.6980_6981delinsCT XP_016865463.1:p.Ser2327=
NR_003149.2:n.6996_6997delinsCT