Canonical Allele Identifier: CA3341561

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90784004A>G , CM000667.2:g.90784004A>G	GRCh38
NC_000005.9:g.90079821A>G , CM000667.1:g.90079821A>G	GRCh37
NC_000005.8:g.90115577A>G	NCBI36
NG_007083.1:g.230205A>G
NG_007083.2:g.259661A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13600A>G MANE Select	NP_115495.3:p.Met4534Val
ENST00000405460.9:c.13600A>G MANE Select	ENSP00000384582.2:p.Met4534Val
NM_032119.3:c.13600A>G	NP_115495.3:p.Met4534Val
NR_003149.1:n.13613A>G
NR_003149.2:n.13616A>G
ENST00000405460.6:c.13600A>G	ENSP00000384582.2:p.Met4534Val
ENST00000425867.2:c.583A>G	ENSP00000392618.2:p.Met195Val
ENST00000425867.3:c.2554A>G	ENSP00000392618.3:p.Met852Val
ENST00000638510.1:n.867A>G
ENST00000638975.1:c.229A>G	ENSP00000492630.1:p.Met77Val
ENST00000639431.1:c.265+107795A>G	ENSP00000491057.1:n.265+107795A>G
ENST00000640407.1:c.10A>G	ENSP00000491425.1:p.Met4Val
XM_011543675.1:c.13597A>G	XP_011541977.1:p.Met4533Val
XM_011543676.1:c.13519A>G	XP_011541978.1:p.Met4507Val
XM_011543677.1:c.10903A>G	XP_011541979.1:p.Met3635Val
XM_011543678.1:c.13600A>G	XP_011541980.1:p.Met4534Val
XM_017009963.2:c.13621A>G	XP_016865452.1:p.Met4541Val
XM_017009964.2:c.13618A>G	XP_016865453.1:p.Met4540Val
XM_017009965.1:c.13618A>G	XP_016865454.1:p.Met4540Val
XM_017009966.2:c.13540A>G	XP_016865455.1:p.Met4514Val
XM_017009967.1:c.13525A>G	XP_016865456.1:p.Met4509Val
XM_017009968.2:c.13621A>G	XP_016865457.1:p.Met4541Val
XM_017009969.2:c.13621A>G	XP_016865458.1:p.Met4541Val
XM_017009970.2:c.13621A>G	XP_016865459.1:p.Met4541Val
XM_017009971.2:c.13621A>G	XP_016865460.1:p.Met4541Val
XM_017009972.1:c.6739A>G	XP_016865461.1:p.Met2247Val
XM_017009973.1:c.6718A>G	XP_016865462.1:p.Met2240Val