Canonical Allele Identifier: CA360397519

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012458T>A (hg19) ; chr5:g.90716641T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716641T>A , CM000667.2:g.90716641T>A	GRCh38
NC_000005.9:g.90012458T>A , CM000667.1:g.90012458T>A	GRCh37
NC_000005.8:g.90048214T>A	NCBI36
NG_007083.1:g.162842T>A
NG_007083.2:g.192298T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9359T>A MANE Select	ENSP00000384582.2:p.Ile3120Asn
ENST00000639431.1:c.265+40432T>A	ENSP00000491057.1:n.265+40432T>A
ENST00000639473.1:n.4818T>A
ENST00000640012.1:c.3166T>A
ENST00000640374.1:n.2503T>A
ENST00000640779.1:c.4088T>A
ENST00000405460.6:c.9359T>A	ENSP00000384582.2:p.Ile3120Asn
ENST00000509621.1:c.2056T>A
NM_032119.3:c.9359T>A	NP_115495.3:p.Ile3120Asn
NR_003149.1:n.9372T>A
XM_011543675.1:c.9356T>A	XP_011541977.1:p.Ile3119Asn
XM_011543676.1:c.9278T>A	XP_011541978.1:p.Ile3093Asn
XM_011543677.1:c.6662T>A	XP_011541979.1:p.Ile2221Asn
XM_011543678.1:c.9359T>A	XP_011541980.1:p.Ile3120Asn
XM_011543679.1:c.9359T>A	XP_011541981.1:p.Ile3120Asn
XR_948560.1:n.272-832A>T
NM_032119.4:c.9359T>A MANE Select	NP_115495.3:p.Ile3120Asn
XM_017009963.2:c.9380T>A	XP_016865452.1:p.Ile3127Asn
XM_017009964.2:c.9377T>A	XP_016865453.1:p.Ile3126Asn
XM_017009965.1:c.9377T>A	XP_016865454.1:p.Ile3126Asn
XM_017009966.2:c.9299T>A	XP_016865455.1:p.Ile3100Asn
XM_017009967.1:c.9284T>A	XP_016865456.1:p.Ile3095Asn
XM_017009968.2:c.9380T>A	XP_016865457.1:p.Ile3127Asn
XM_017009969.2:c.9380T>A	XP_016865458.1:p.Ile3127Asn
XM_017009970.2:c.9380T>A	XP_016865459.1:p.Ile3127Asn
XM_017009971.2:c.9380T>A	XP_016865460.1:p.Ile3127Asn
XM_017009972.1:c.2498T>A	XP_016865461.1:p.Ile833Asn
XM_017009973.1:c.2477T>A	XP_016865462.1:p.Ile826Asn
XM_017009974.2:c.9380T>A	XP_016865463.1:p.Ile3127Asn
XR_001742802.1:n.2523-832A>T
NR_003149.2:n.9375T>A