Canonical Allele Identifier: CA360397737

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012518T>A (hg19) ; chr5:g.90716701T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716701T>A , CM000667.2:g.90716701T>A	GRCh38
NC_000005.9:g.90012518T>A , CM000667.1:g.90012518T>A	GRCh37
NC_000005.8:g.90048274T>A	NCBI36
NG_007083.1:g.162902T>A
NG_007083.2:g.192358T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9419T>A MANE Select	ENSP00000384582.2:p.Ile3140Asn
ENST00000639431.1:c.265+40492T>A	ENSP00000491057.1:n.265+40492T>A
ENST00000639473.1:n.4878T>A
ENST00000640012.1:c.3226T>A
ENST00000640374.1:n.2563T>A
ENST00000640779.1:c.4148T>A
ENST00000405460.6:c.9419T>A	ENSP00000384582.2:p.Ile3140Asn
ENST00000509621.1:c.2116T>A
NM_032119.3:c.9419T>A	NP_115495.3:p.Ile3140Asn
NR_003149.1:n.9432T>A
XM_011543675.1:c.9416T>A	XP_011541977.1:p.Ile3139Asn
XM_011543676.1:c.9338T>A	XP_011541978.1:p.Ile3113Asn
XM_011543677.1:c.6722T>A	XP_011541979.1:p.Ile2241Asn
XM_011543678.1:c.9419T>A	XP_011541980.1:p.Ile3140Asn
XM_011543679.1:c.9419T>A	XP_011541981.1:p.Ile3140Asn
XR_948560.1:n.272-892A>T
NM_032119.4:c.9419T>A MANE Select	NP_115495.3:p.Ile3140Asn
XM_017009963.2:c.9440T>A	XP_016865452.1:p.Ile3147Asn
XM_017009964.2:c.9437T>A	XP_016865453.1:p.Ile3146Asn
XM_017009965.1:c.9437T>A	XP_016865454.1:p.Ile3146Asn
XM_017009966.2:c.9359T>A	XP_016865455.1:p.Ile3120Asn
XM_017009967.1:c.9344T>A	XP_016865456.1:p.Ile3115Asn
XM_017009968.2:c.9440T>A	XP_016865457.1:p.Ile3147Asn
XM_017009969.2:c.9440T>A	XP_016865458.1:p.Ile3147Asn
XM_017009970.2:c.9440T>A	XP_016865459.1:p.Ile3147Asn
XM_017009971.2:c.9440T>A	XP_016865460.1:p.Ile3147Asn
XM_017009972.1:c.2558T>A	XP_016865461.1:p.Ile853Asn
XM_017009973.1:c.2537T>A	XP_016865462.1:p.Ile846Asn
XM_017009974.2:c.9440T>A	XP_016865463.1:p.Ile3147Asn
XR_001742802.1:n.2523-892A>T
NR_003149.2:n.9435T>A