Canonical Allele Identifier: CA360385083

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1242852645
• MyVariant Identifiers: chr5:g.89913645T>G (hg19) ; chr5:g.90617828T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617828T>G , CM000667.2:g.90617828T>G	GRCh38
NC_000005.9:g.89913645T>G , CM000667.1:g.89913645T>G	GRCh37
NC_000005.8:g.89949401T>G	NCBI36
NG_007083.1:g.64029T>G
NG_007083.2:g.93485T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.232T>G MANE Select	ENSP00000384582.2:p.Phe78Val
ENST00000638316.1:n.442T>G
ENST00000638638.1:n.639T>G
ENST00000640109.1:n.328T>G
ENST00000640281.1:n.291T>G
ENST00000405460.6:c.232T>G	ENSP00000384582.2:p.Phe78Val
ENST00000508842.5:c.244T>G	ENSP00000425936.1:p.Phe82Val
NM_032119.3:c.232T>G	NP_115495.3:p.Phe78Val
NR_003149.1:n.328T>G
XM_011543675.1:c.232T>G	XP_011541977.1:p.Phe78Val
XM_011543676.1:c.232T>G	XP_011541978.1:p.Phe78Val
XM_011543678.1:c.232T>G	XP_011541980.1:p.Phe78Val
XM_011543679.1:c.232T>G	XP_011541981.1:p.Phe78Val
NM_032119.4:c.232T>G MANE Select	NP_115495.3:p.Phe78Val
XM_017009963.2:c.232T>G	XP_016865452.1:p.Phe78Val
XM_017009964.2:c.232T>G	XP_016865453.1:p.Phe78Val
XM_017009965.1:c.229T>G	XP_016865454.1:p.Phe77Val
XM_017009966.2:c.232T>G	XP_016865455.1:p.Phe78Val
XM_017009967.1:c.232T>G	XP_016865456.1:p.Phe78Val
XM_017009968.2:c.232T>G	XP_016865457.1:p.Phe78Val
XM_017009969.2:c.232T>G	XP_016865458.1:p.Phe78Val
XM_017009970.2:c.232T>G	XP_016865459.1:p.Phe78Val
XM_017009971.2:c.232T>G	XP_016865460.1:p.Phe78Val
XM_017009974.2:c.232T>G	XP_016865463.1:p.Phe78Val
NR_003149.2:n.331T>G