Canonical Allele Identifier: CA360366688

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050885T>A (hg19) ; chr5:g.90755068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755068T>A , CM000667.2:g.90755068T>A	GRCh38
NC_000005.9:g.90050885T>A , CM000667.1:g.90050885T>A	GRCh37
NC_000005.8:g.90086641T>A	NCBI36
NG_007083.1:g.201269T>A
NG_007083.2:g.230725T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11463T>A MANE Select	ENSP00000384582.2:p.Asn3821Lys
ENST00000425867.3:c.594T>A	ENSP00000392618.3:p.Asn198Lys
ENST00000639431.1:c.265+78859T>A	ENSP00000491057.1:n.265+78859T>A
ENST00000640374.1:n.4607T>A
ENST00000640464.1:n.1882T>A
ENST00000405460.6:c.11463T>A	ENSP00000384582.2:p.Asn3821Lys
ENST00000509621.1:c.4160T>A
NM_032119.3:c.11463T>A	NP_115495.3:p.Asn3821Lys
NR_003149.1:n.11476T>A
XM_011543675.1:c.11460T>A	XP_011541977.1:p.Asn3820Lys
XM_011543676.1:c.11382T>A	XP_011541978.1:p.Asn3794Lys
XM_011543677.1:c.8766T>A	XP_011541979.1:p.Asn2922Lys
XM_011543678.1:c.11463T>A	XP_011541980.1:p.Asn3821Lys
NM_032119.4:c.11463T>A MANE Select	NP_115495.3:p.Asn3821Lys
XM_017009963.2:c.11484T>A	XP_016865452.1:p.Asn3828Lys
XM_017009964.2:c.11481T>A	XP_016865453.1:p.Asn3827Lys
XM_017009965.1:c.11481T>A	XP_016865454.1:p.Asn3827Lys
XM_017009966.2:c.11403T>A	XP_016865455.1:p.Asn3801Lys
XM_017009967.1:c.11388T>A	XP_016865456.1:p.Asn3796Lys
XM_017009968.2:c.11484T>A	XP_016865457.1:p.Asn3828Lys
XM_017009969.2:c.11484T>A	XP_016865458.1:p.Asn3828Lys
XM_017009970.2:c.11484T>A	XP_016865459.1:p.Asn3828Lys
XM_017009971.2:c.11484T>A	XP_016865460.1:p.Asn3828Lys
XM_017009972.1:c.4602T>A	XP_016865461.1:p.Asn1534Lys
XM_017009973.1:c.4581T>A	XP_016865462.1:p.Asn1527Lys
NR_003149.2:n.11479T>A