Canonical Allele Identifier: CA360367456

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050995T>A (hg19) ; chr5:g.90755178T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755178T>A , CM000667.2:g.90755178T>A	GRCh38
NC_000005.9:g.90050995T>A , CM000667.1:g.90050995T>A	GRCh37
NC_000005.8:g.90086751T>A	NCBI36
NG_007083.1:g.201379T>A
NG_007083.2:g.230835T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11573T>A MANE Select	ENSP00000384582.2:p.Ile3858Asn
ENST00000425867.3:c.704T>A	ENSP00000392618.3:p.Ile235Asn
ENST00000639431.1:c.265+78969T>A	ENSP00000491057.1:n.265+78969T>A
ENST00000640374.1:n.4717T>A
ENST00000640464.1:n.1992T>A
ENST00000405460.6:c.11573T>A	ENSP00000384582.2:p.Ile3858Asn
ENST00000509621.1:c.4270T>A
NM_032119.3:c.11573T>A	NP_115495.3:p.Ile3858Asn
NR_003149.1:n.11586T>A
XM_011543675.1:c.11570T>A	XP_011541977.1:p.Ile3857Asn
XM_011543676.1:c.11492T>A	XP_011541978.1:p.Ile3831Asn
XM_011543677.1:c.8876T>A	XP_011541979.1:p.Ile2959Asn
XM_011543678.1:c.11573T>A	XP_011541980.1:p.Ile3858Asn
NM_032119.4:c.11573T>A MANE Select	NP_115495.3:p.Ile3858Asn
XM_017009963.2:c.11594T>A	XP_016865452.1:p.Ile3865Asn
XM_017009964.2:c.11591T>A	XP_016865453.1:p.Ile3864Asn
XM_017009965.1:c.11591T>A	XP_016865454.1:p.Ile3864Asn
XM_017009966.2:c.11513T>A	XP_016865455.1:p.Ile3838Asn
XM_017009967.1:c.11498T>A	XP_016865456.1:p.Ile3833Asn
XM_017009968.2:c.11594T>A	XP_016865457.1:p.Ile3865Asn
XM_017009969.2:c.11594T>A	XP_016865458.1:p.Ile3865Asn
XM_017009970.2:c.11594T>A	XP_016865459.1:p.Ile3865Asn
XM_017009971.2:c.11594T>A	XP_016865460.1:p.Ile3865Asn
XM_017009972.1:c.4712T>A	XP_016865461.1:p.Ile1571Asn
XM_017009973.1:c.4691T>A	XP_016865462.1:p.Ile1564Asn
NR_003149.2:n.11589T>A