Canonical Allele Identifier: CA2767420574
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692840_90692844del , CM000667.2:g.90692840_90692844del GRCh38
NC_000005.9:g.89988657_89988661del , CM000667.1:g.89988657_89988661del GRCh37
NC_000005.8:g.90024413_90024417del NCBI36
NG_007083.1:g.139041_139045del
NG_007083.2:g.168497_168501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+54_7133+58del MANE Select ENSP00000384582.2:n.7133+54_7133+58del
ENST00000639431.1:c.265+16631_265+16635del ENSP00000491057.1:n.265+16631_265+16635del
ENST00000639473.1:n.2592+54_2592+58del
ENST00000640012.1:c.940+54_940+58del
ENST00000640374.1:n.277+54_277+58del
ENST00000640403.1:c.4424+54_4424+58del ENSP00000492531.1:n.4424+54_4424+58del
ENST00000640779.1:c.1862+54_1862+58del
ENST00000405460.6:c.7133+54_7133+58del ENSP00000384582.2:n.7133+54_7133+58del
NM_032119.3:c.7133+54_7133+58del NP_115495.3:n.7133+54_7133+58del
NR_003149.1:n.7146+54_7146+58del
XM_011543675.1:c.7130+54_7130+58del XP_011541977.1:n.7130+54_7130+58del
XM_011543676.1:c.7052+54_7052+58del XP_011541978.1:n.7052+54_7052+58del
XM_011543677.1:c.4436+54_4436+58del XP_011541979.1:n.4436+54_4436+58del
XM_011543678.1:c.7133+54_7133+58del XP_011541980.1:n.7133+54_7133+58del
XM_011543679.1:c.7133+54_7133+58del XP_011541981.1:n.7133+54_7133+58del
NM_032119.4:c.7133+54_7133+58del MANE Select NP_115495.3:n.7133+54_7133+58del
XM_017009963.2:c.7133+54_7133+58del XP_016865452.1:n.7133+54_7133+58del
XM_017009964.2:c.7130+54_7130+58del XP_016865453.1:n.7130+54_7130+58del
XM_017009965.1:c.7130+54_7130+58del XP_016865454.1:n.7130+54_7130+58del
XM_017009966.2:c.7052+54_7052+58del XP_016865455.1:n.7052+54_7052+58del
XM_017009967.1:c.7037+54_7037+58del XP_016865456.1:n.7037+54_7037+58del
XM_017009968.2:c.7133+54_7133+58del XP_016865457.1:n.7133+54_7133+58del
XM_017009969.2:c.7133+54_7133+58del XP_016865458.1:n.7133+54_7133+58del
XM_017009970.2:c.7133+54_7133+58del XP_016865459.1:n.7133+54_7133+58del
XM_017009971.2:c.7133+54_7133+58del XP_016865460.1:n.7133+54_7133+58del
XM_017009972.1:c.251+54_251+58del XP_016865461.1:n.251+54_251+58del
XM_017009973.1:c.251+54_251+58del XP_016865462.1:n.251+54_251+58del
XM_017009974.2:c.7133+54_7133+58del XP_016865463.1:n.7133+54_7133+58del
NR_003149.2:n.7149+54_7149+58del