Canonical Allele Identifier: CA360366332

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050828A>G (hg19) ; chr5:g.90755011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755011A>G , CM000667.2:g.90755011A>G	GRCh38
NC_000005.9:g.90050828A>G , CM000667.1:g.90050828A>G	GRCh37
NC_000005.8:g.90086584A>G	NCBI36
NG_007083.1:g.201212A>G
NG_007083.2:g.230668A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11406A>G MANE Select	ENSP00000384582.2:p.Ile3802Met
ENST00000425867.3:c.537A>G	ENSP00000392618.3:p.Ile179Met
ENST00000639431.1:c.265+78802A>G	ENSP00000491057.1:n.265+78802A>G
ENST00000640374.1:n.4550A>G
ENST00000640464.1:n.1825A>G
ENST00000405460.6:c.11406A>G	ENSP00000384582.2:p.Ile3802Met
ENST00000509621.1:c.4103A>G
NM_032119.3:c.11406A>G	NP_115495.3:p.Ile3802Met
NR_003149.1:n.11419A>G
XM_011543675.1:c.11403A>G	XP_011541977.1:p.Ile3801Met
XM_011543676.1:c.11325A>G	XP_011541978.1:p.Ile3775Met
XM_011543677.1:c.8709A>G	XP_011541979.1:p.Ile2903Met
XM_011543678.1:c.11406A>G	XP_011541980.1:p.Ile3802Met
NM_032119.4:c.11406A>G MANE Select	NP_115495.3:p.Ile3802Met
XM_017009963.2:c.11427A>G	XP_016865452.1:p.Ile3809Met
XM_017009964.2:c.11424A>G	XP_016865453.1:p.Ile3808Met
XM_017009965.1:c.11424A>G	XP_016865454.1:p.Ile3808Met
XM_017009966.2:c.11346A>G	XP_016865455.1:p.Ile3782Met
XM_017009967.1:c.11331A>G	XP_016865456.1:p.Ile3777Met
XM_017009968.2:c.11427A>G	XP_016865457.1:p.Ile3809Met
XM_017009969.2:c.11427A>G	XP_016865458.1:p.Ile3809Met
XM_017009970.2:c.11427A>G	XP_016865459.1:p.Ile3809Met
XM_017009971.2:c.11427A>G	XP_016865460.1:p.Ile3809Met
XM_017009972.1:c.4545A>G	XP_016865461.1:p.Ile1515Met
XM_017009973.1:c.4524A>G	XP_016865462.1:p.Ile1508Met
NR_003149.2:n.11422A>G