Canonical Allele Identifier: CA360408819

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041421A>G (hg19) ; chr5:g.90745604A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745604A>G , CM000667.2:g.90745604A>G	GRCh38
NC_000005.9:g.90041421A>G , CM000667.1:g.90041421A>G	GRCh37
NC_000005.8:g.90077177A>G	NCBI36
NG_007083.1:g.191805A>G
NG_007083.2:g.221261A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10783A>G MANE Select	ENSP00000384582.2:p.Ile3595Val
ENST00000639431.1:c.265+69395A>G	ENSP00000491057.1:n.265+69395A>G
ENST00000640374.1:n.3927A>G
ENST00000640464.1:n.1202A>G
ENST00000405460.6:c.10783A>G	ENSP00000384582.2:p.Ile3595Val
ENST00000509621.1:c.3480A>G
NM_032119.3:c.10783A>G	NP_115495.3:p.Ile3595Val
NR_003149.1:n.10796A>G
XM_011543675.1:c.10780A>G	XP_011541977.1:p.Ile3594Val
XM_011543676.1:c.10702A>G	XP_011541978.1:p.Ile3568Val
XM_011543677.1:c.8086A>G	XP_011541979.1:p.Ile2696Val
XM_011543678.1:c.10783A>G	XP_011541980.1:p.Ile3595Val
XM_011543679.1:c.*5A>G	XP_011541981.1:n.*5A>G
NM_032119.4:c.10783A>G MANE Select	NP_115495.3:p.Ile3595Val
XM_017009963.2:c.10804A>G	XP_016865452.1:p.Ile3602Val
XM_017009964.2:c.10801A>G	XP_016865453.1:p.Ile3601Val
XM_017009965.1:c.10801A>G	XP_016865454.1:p.Ile3601Val
XM_017009966.2:c.10723A>G	XP_016865455.1:p.Ile3575Val
XM_017009967.1:c.10708A>G	XP_016865456.1:p.Ile3570Val
XM_017009968.2:c.10804A>G	XP_016865457.1:p.Ile3602Val
XM_017009969.2:c.10804A>G	XP_016865458.1:p.Ile3602Val
XM_017009970.2:c.10804A>G	XP_016865459.1:p.Ile3602Val
XM_017009971.2:c.10804A>G	XP_016865460.1:p.Ile3602Val
XM_017009972.1:c.3922A>G	XP_016865461.1:p.Ile1308Val
XM_017009973.1:c.3901A>G	XP_016865462.1:p.Ile1301Val
XM_017009974.2:c.*5A>G	XP_016865463.1:n.*5A>G
NR_003149.2:n.10799A>G