Canonical Allele Identifier: CA360408962

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041455C>G (hg19) ; chr5:g.90745638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745638C>G , CM000667.2:g.90745638C>G	GRCh38
NC_000005.9:g.90041455C>G , CM000667.1:g.90041455C>G	GRCh37
NC_000005.8:g.90077211C>G	NCBI36
NG_007083.1:g.191839C>G
NG_007083.2:g.221295C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10817C>G MANE Select	ENSP00000384582.2:p.Ala3606Gly
ENST00000639431.1:c.265+69429C>G	ENSP00000491057.1:n.265+69429C>G
ENST00000640374.1:n.3961C>G
ENST00000640464.1:n.1236C>G
ENST00000405460.6:c.10817C>G	ENSP00000384582.2:p.Ala3606Gly
ENST00000509621.1:c.3514C>G
NM_032119.3:c.10817C>G	NP_115495.3:p.Ala3606Gly
NR_003149.1:n.10830C>G
XM_011543675.1:c.10814C>G	XP_011541977.1:p.Ala3605Gly
XM_011543676.1:c.10736C>G	XP_011541978.1:p.Ala3579Gly
XM_011543677.1:c.8120C>G	XP_011541979.1:p.Ala2707Gly
XM_011543678.1:c.10817C>G	XP_011541980.1:p.Ala3606Gly
XM_011543679.1:c.*39C>G	XP_011541981.1:n.*39C>G
NM_032119.4:c.10817C>G MANE Select	NP_115495.3:p.Ala3606Gly
XM_017009963.2:c.10838C>G	XP_016865452.1:p.Ala3613Gly
XM_017009964.2:c.10835C>G	XP_016865453.1:p.Ala3612Gly
XM_017009965.1:c.10835C>G	XP_016865454.1:p.Ala3612Gly
XM_017009966.2:c.10757C>G	XP_016865455.1:p.Ala3586Gly
XM_017009967.1:c.10742C>G	XP_016865456.1:p.Ala3581Gly
XM_017009968.2:c.10838C>G	XP_016865457.1:p.Ala3613Gly
XM_017009969.2:c.10838C>G	XP_016865458.1:p.Ala3613Gly
XM_017009970.2:c.10838C>G	XP_016865459.1:p.Ala3613Gly
XM_017009971.2:c.10838C>G	XP_016865460.1:p.Ala3613Gly
XM_017009972.1:c.3956C>G	XP_016865461.1:p.Ala1319Gly
XM_017009973.1:c.3935C>G	XP_016865462.1:p.Ala1312Gly
XM_017009974.2:c.*39C>G	XP_016865463.1:n.*39C>G
NR_003149.2:n.10833C>G