Canonical Allele Identifier: CA360385122

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89913648T>G (hg19) ; chr5:g.90617831T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617831T>G , CM000667.2:g.90617831T>G	GRCh38
NC_000005.9:g.89913648T>G , CM000667.1:g.89913648T>G	GRCh37
NC_000005.8:g.89949404T>G	NCBI36
NG_007083.1:g.64032T>G
NG_007083.2:g.93488T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.235T>G MANE Select	ENSP00000384582.2:p.Phe79Val
ENST00000638316.1:n.445T>G
ENST00000638638.1:n.642T>G
ENST00000640109.1:n.331T>G
ENST00000640281.1:n.294T>G
ENST00000405460.6:c.235T>G	ENSP00000384582.2:p.Phe79Val
ENST00000508842.5:c.247T>G	ENSP00000425936.1:p.Phe83Val
NM_032119.3:c.235T>G	NP_115495.3:p.Phe79Val
NR_003149.1:n.331T>G
XM_011543675.1:c.235T>G	XP_011541977.1:p.Phe79Val
XM_011543676.1:c.235T>G	XP_011541978.1:p.Phe79Val
XM_011543678.1:c.235T>G	XP_011541980.1:p.Phe79Val
XM_011543679.1:c.235T>G	XP_011541981.1:p.Phe79Val
NM_032119.4:c.235T>G MANE Select	NP_115495.3:p.Phe79Val
XM_017009963.2:c.235T>G	XP_016865452.1:p.Phe79Val
XM_017009964.2:c.235T>G	XP_016865453.1:p.Phe79Val
XM_017009965.1:c.232T>G	XP_016865454.1:p.Phe78Val
XM_017009966.2:c.235T>G	XP_016865455.1:p.Phe79Val
XM_017009967.1:c.235T>G	XP_016865456.1:p.Phe79Val
XM_017009968.2:c.235T>G	XP_016865457.1:p.Phe79Val
XM_017009969.2:c.235T>G	XP_016865458.1:p.Phe79Val
XM_017009970.2:c.235T>G	XP_016865459.1:p.Phe79Val
XM_017009971.2:c.235T>G	XP_016865460.1:p.Phe79Val
XM_017009974.2:c.235T>G	XP_016865463.1:p.Phe79Val
NR_003149.2:n.334T>G