Canonical Allele Identifier: CA360378308

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763412A>G , CM000667.2:g.90763412A>G	GRCh38
NC_000005.9:g.90059229A>G , CM000667.1:g.90059229A>G	GRCh37
NC_000005.8:g.90094985A>G	NCBI36
NG_007083.1:g.209613A>G
NG_007083.2:g.239069A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12228A>G MANE Select	NP_115495.3:p.Ile4076Met
ENST00000405460.9:c.12228A>G MANE Select	ENSP00000384582.2:p.Ile4076Met
NM_032119.3:c.12228A>G	NP_115495.3:p.Ile4076Met
NR_003149.1:n.12241A>G
NR_003149.2:n.12244A>G
ENST00000405460.6:c.12228A>G	ENSP00000384582.2:p.Ile4076Met
ENST00000425867.3:c.1182A>G	ENSP00000392618.3:p.Ile394Met
ENST00000639431.1:c.265+87203A>G	ENSP00000491057.1:n.265+87203A>G
ENST00000640464.1:n.2647A>G
ENST00000640729.1:n.805A>G
XM_011543675.1:c.12225A>G	XP_011541977.1:p.Ile4075Met
XM_011543676.1:c.12147A>G	XP_011541978.1:p.Ile4049Met
XM_011543677.1:c.9531A>G	XP_011541979.1:p.Ile3177Met
XM_011543678.1:c.12228A>G	XP_011541980.1:p.Ile4076Met
XM_017009963.2:c.12249A>G	XP_016865452.1:p.Ile4083Met
XM_017009964.2:c.12246A>G	XP_016865453.1:p.Ile4082Met
XM_017009965.1:c.12246A>G	XP_016865454.1:p.Ile4082Met
XM_017009966.2:c.12168A>G	XP_016865455.1:p.Ile4056Met
XM_017009967.1:c.12153A>G	XP_016865456.1:p.Ile4051Met
XM_017009968.2:c.12249A>G	XP_016865457.1:p.Ile4083Met
XM_017009969.2:c.12249A>G	XP_016865458.1:p.Ile4083Met
XM_017009970.2:c.12249A>G	XP_016865459.1:p.Ile4083Met
XM_017009971.2:c.12249A>G	XP_016865460.1:p.Ile4083Met
XM_017009972.1:c.5367A>G	XP_016865461.1:p.Ile1789Met
XM_017009973.1:c.5346A>G	XP_016865462.1:p.Ile1782Met