Canonical Allele Identifier: CA360401649

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087011C>G (hg19) ; chr5:g.90791194C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791194C>G , CM000667.2:g.90791194C>G	GRCh38
NC_000005.9:g.90087011C>G , CM000667.1:g.90087011C>G	GRCh37
NC_000005.8:g.90122767C>G	NCBI36
NG_007083.1:g.237395C>G
NG_007083.2:g.266851C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14365C>G MANE Select	ENSP00000384582.2:p.Arg4789Gly
ENST00000425867.3:c.3319C>G	ENSP00000392618.3:p.Arg1107Gly
ENST00000507314.2:c.40C>G	ENSP00000491299.1:p.Arg14Gly
ENST00000638510.1:n.1632C>G
ENST00000638585.1:n.131C>G
ENST00000638975.1:c.994C>G	ENSP00000492630.1:p.Arg332Gly
ENST00000639431.1:c.265+114985C>G	ENSP00000491057.1:n.265+114985C>G
ENST00000640407.1:c.775C>G	ENSP00000491425.1:p.Arg259Gly
ENST00000405460.6:c.14365C>G	ENSP00000384582.2:p.Arg4789Gly
ENST00000425867.2:c.1348C>G	ENSP00000392618.2:p.Arg450Gly
ENST00000507314.1:n.40C>G
NM_032119.3:c.14365C>G	NP_115495.3:p.Arg4789Gly
NR_003149.1:n.14378C>G
XM_011543675.1:c.14362C>G	XP_011541977.1:p.Arg4788Gly
XM_011543676.1:c.14284C>G	XP_011541978.1:p.Arg4762Gly
XM_011543677.1:c.11668C>G	XP_011541979.1:p.Arg3890Gly
XM_011543678.1:c.14365C>G	XP_011541980.1:p.Arg4789Gly
NM_032119.4:c.14365C>G MANE Select	NP_115495.3:p.Arg4789Gly
XM_017009963.2:c.14386C>G	XP_016865452.1:p.Arg4796Gly
XM_017009964.2:c.14383C>G	XP_016865453.1:p.Arg4795Gly
XM_017009965.1:c.14383C>G	XP_016865454.1:p.Arg4795Gly
XM_017009966.2:c.14305C>G	XP_016865455.1:p.Arg4769Gly
XM_017009967.1:c.14290C>G	XP_016865456.1:p.Arg4764Gly
XM_017009968.2:c.14386C>G	XP_016865457.1:p.Arg4796Gly
XM_017009969.2:c.14386C>G	XP_016865458.1:p.Arg4796Gly
XM_017009970.2:c.14386C>G	XP_016865459.1:p.Arg4796Gly
XM_017009971.2:c.14386C>G	XP_016865460.1:p.Arg4796Gly
XM_017009972.1:c.7504C>G	XP_016865461.1:p.Arg2502Gly
XM_017009973.1:c.7483C>G	XP_016865462.1:p.Arg2495Gly
NR_003149.2:n.14381C>G