Canonical Allele Identifier: CA360403200

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021384C>G (hg19) ; chr5:g.90725567C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725567C>G , CM000667.2:g.90725567C>G	GRCh38
NC_000005.9:g.90021384C>G , CM000667.1:g.90021384C>G	GRCh37
NC_000005.8:g.90057140C>G	NCBI36
NG_007083.1:g.171768C>G
NG_007083.2:g.201224C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10072C>G MANE Select	ENSP00000384582.2:p.Leu3358Val
ENST00000639431.1:c.265+49358C>G	ENSP00000491057.1:n.265+49358C>G
ENST00000640374.1:n.3216C>G
ENST00000640464.1:n.491C>G
ENST00000405460.6:c.10072C>G	ENSP00000384582.2:p.Leu3358Val
ENST00000509621.1:c.2769C>G
NM_032119.3:c.10072C>G	NP_115495.3:p.Leu3358Val
NR_003149.1:n.10085C>G
XM_011543675.1:c.10069C>G	XP_011541977.1:p.Leu3357Val
XM_011543676.1:c.9991C>G	XP_011541978.1:p.Leu3331Val
XM_011543677.1:c.7375C>G	XP_011541979.1:p.Leu2459Val
XM_011543678.1:c.10072C>G	XP_011541980.1:p.Leu3358Val
XM_011543679.1:c.10072C>G	XP_011541981.1:p.Leu3358Val
XR_948560.1:n.272-9758G>C
NM_032119.4:c.10072C>G MANE Select	NP_115495.3:p.Leu3358Val
XM_017009963.2:c.10093C>G	XP_016865452.1:p.Leu3365Val
XM_017009964.2:c.10090C>G	XP_016865453.1:p.Leu3364Val
XM_017009965.1:c.10090C>G	XP_016865454.1:p.Leu3364Val
XM_017009966.2:c.10012C>G	XP_016865455.1:p.Leu3338Val
XM_017009967.1:c.9997C>G	XP_016865456.1:p.Leu3333Val
XM_017009968.2:c.10093C>G	XP_016865457.1:p.Leu3365Val
XM_017009969.2:c.10093C>G	XP_016865458.1:p.Leu3365Val
XM_017009970.2:c.10093C>G	XP_016865459.1:p.Leu3365Val
XM_017009971.2:c.10093C>G	XP_016865460.1:p.Leu3365Val
XM_017009972.1:c.3211C>G	XP_016865461.1:p.Leu1071Val
XM_017009973.1:c.3190C>G	XP_016865462.1:p.Leu1064Val
XM_017009974.2:c.10093C>G	XP_016865463.1:p.Leu3365Val
XR_001742802.1:n.2523-9758G>C
NR_003149.2:n.10088C>G