Canonical Allele Identifier: CA360363061

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90622621-C-G
• MyVariant Identifiers: chr5:g.89918438C>G (hg19) ; chr5:g.90622621C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90622621C>G , CM000667.2:g.90622621C>G	GRCh38
NC_000005.9:g.89918438C>G , CM000667.1:g.89918438C>G	GRCh37
NC_000005.8:g.89954194C>G	NCBI36
NG_007083.1:g.68822C>G
NG_007083.2:g.98278C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.478C>G MANE Select	ENSP00000384582.2:p.Pro160Ala
ENST00000638316.1:n.688C>G
ENST00000638638.1:n.885C>G
ENST00000640083.1:n.183C>G
ENST00000640109.1:n.574C>G
ENST00000640281.1:n.537C>G
ENST00000405460.6:c.478C>G	ENSP00000384582.2:p.Pro160Ala
ENST00000508842.5:c.394C>G	ENSP00000425936.1:p.Pro132Ala
NM_032119.3:c.478C>G	NP_115495.3:p.Pro160Ala
NR_003149.1:n.574C>G
XM_011543675.1:c.478C>G	XP_011541977.1:p.Pro160Ala
XM_011543676.1:c.478C>G	XP_011541978.1:p.Pro160Ala
XM_011543678.1:c.478C>G	XP_011541980.1:p.Pro160Ala
XM_011543679.1:c.478C>G	XP_011541981.1:p.Pro160Ala
NM_032119.4:c.478C>G MANE Select	NP_115495.3:p.Pro160Ala
XM_017009963.2:c.478C>G	XP_016865452.1:p.Pro160Ala
XM_017009964.2:c.478C>G	XP_016865453.1:p.Pro160Ala
XM_017009965.1:c.475C>G	XP_016865454.1:p.Pro159Ala
XM_017009966.2:c.478C>G	XP_016865455.1:p.Pro160Ala
XM_017009967.1:c.382C>G	XP_016865456.1:p.Pro128Ala
XM_017009968.2:c.478C>G	XP_016865457.1:p.Pro160Ala
XM_017009969.2:c.478C>G	XP_016865458.1:p.Pro160Ala
XM_017009970.2:c.478C>G	XP_016865459.1:p.Pro160Ala
XM_017009971.2:c.478C>G	XP_016865460.1:p.Pro160Ala
XM_017009974.2:c.478C>G	XP_016865463.1:p.Pro160Ala
NR_003149.2:n.577C>G