Canonical Allele Identifier: CA2767420582
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692849_90692850insAGA , CM000667.2:g.90692849_90692850insAGA GRCh38
NC_000005.9:g.89988666_89988667insAGA , CM000667.1:g.89988666_89988667insAGA GRCh37
NC_000005.8:g.90024422_90024423insAGA NCBI36
NG_007083.1:g.139050_139051insAGA
NG_007083.2:g.168506_168507insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+63_7133+64insAGA MANE Select ENSP00000384582.2:n.7133+63_7133+64insAGA
ENST00000639431.1:c.265+16640_265+16641insAGA ENSP00000491057.1:n.265+16640_265+16641insAGA
ENST00000639473.1:n.2592+63_2592+64insAGA
ENST00000640012.1:c.940+63_940+64insAGA
ENST00000640374.1:n.277+63_277+64insAGA
ENST00000640403.1:c.4424+63_4424+64insAGA ENSP00000492531.1:n.4424+63_4424+64insAGA
ENST00000640779.1:c.1862+63_1862+64insAGA
ENST00000405460.6:c.7133+63_7133+64insAGA ENSP00000384582.2:n.7133+63_7133+64insAGA
NM_032119.3:c.7133+63_7133+64insAGA NP_115495.3:n.7133+63_7133+64insAGA
NR_003149.1:n.7146+63_7146+64insAGA
XM_011543675.1:c.7130+63_7130+64insAGA XP_011541977.1:n.7130+63_7130+64insAGA
XM_011543676.1:c.7052+63_7052+64insAGA XP_011541978.1:n.7052+63_7052+64insAGA
XM_011543677.1:c.4436+63_4436+64insAGA XP_011541979.1:n.4436+63_4436+64insAGA
XM_011543678.1:c.7133+63_7133+64insAGA XP_011541980.1:n.7133+63_7133+64insAGA
XM_011543679.1:c.7133+63_7133+64insAGA XP_011541981.1:n.7133+63_7133+64insAGA
NM_032119.4:c.7133+63_7133+64insAGA MANE Select NP_115495.3:n.7133+63_7133+64insAGA
XM_017009963.2:c.7133+63_7133+64insAGA XP_016865452.1:n.7133+63_7133+64insAGA
XM_017009964.2:c.7130+63_7130+64insAGA XP_016865453.1:n.7130+63_7130+64insAGA
XM_017009965.1:c.7130+63_7130+64insAGA XP_016865454.1:n.7130+63_7130+64insAGA
XM_017009966.2:c.7052+63_7052+64insAGA XP_016865455.1:n.7052+63_7052+64insAGA
XM_017009967.1:c.7037+63_7037+64insAGA XP_016865456.1:n.7037+63_7037+64insAGA
XM_017009968.2:c.7133+63_7133+64insAGA XP_016865457.1:n.7133+63_7133+64insAGA
XM_017009969.2:c.7133+63_7133+64insAGA XP_016865458.1:n.7133+63_7133+64insAGA
XM_017009970.2:c.7133+63_7133+64insAGA XP_016865459.1:n.7133+63_7133+64insAGA
XM_017009971.2:c.7133+63_7133+64insAGA XP_016865460.1:n.7133+63_7133+64insAGA
XM_017009972.1:c.251+63_251+64insAGA XP_016865461.1:n.251+63_251+64insAGA
XM_017009973.1:c.251+63_251+64insAGA XP_016865462.1:n.251+63_251+64insAGA
XM_017009974.2:c.7133+63_7133+64insAGA XP_016865463.1:n.7133+63_7133+64insAGA
NR_003149.2:n.7149+63_7149+64insAGA