Canonical Allele Identifier: CA360398887

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085594C>G (hg19) ; chr5:g.90789777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789777C>G , CM000667.2:g.90789777C>G	GRCh38
NC_000005.9:g.90085594C>G , CM000667.1:g.90085594C>G	GRCh37
NC_000005.8:g.90121350C>G	NCBI36
NG_007083.1:g.235978C>G
NG_007083.2:g.265434C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13969C>G MANE Select	ENSP00000384582.2:p.Pro4657Ala
ENST00000425867.3:c.2923C>G	ENSP00000392618.3:p.Pro975Ala
ENST00000638510.1:n.1236C>G
ENST00000638975.1:c.598C>G	ENSP00000492630.1:p.Pro200Ala
ENST00000639431.1:c.265+113568C>G	ENSP00000491057.1:n.265+113568C>G
ENST00000640407.1:c.379C>G	ENSP00000491425.1:p.Pro127Ala
ENST00000405460.6:c.13969C>G	ENSP00000384582.2:p.Pro4657Ala
ENST00000425867.2:c.952C>G	ENSP00000392618.2:p.Pro318Ala
NM_032119.3:c.13969C>G	NP_115495.3:p.Pro4657Ala
NR_003149.1:n.13982C>G
XM_011543675.1:c.13966C>G	XP_011541977.1:p.Pro4656Ala
XM_011543676.1:c.13888C>G	XP_011541978.1:p.Pro4630Ala
XM_011543677.1:c.11272C>G	XP_011541979.1:p.Pro3758Ala
XM_011543678.1:c.13969C>G	XP_011541980.1:p.Pro4657Ala
NM_032119.4:c.13969C>G MANE Select	NP_115495.3:p.Pro4657Ala
XM_017009963.2:c.13990C>G	XP_016865452.1:p.Pro4664Ala
XM_017009964.2:c.13987C>G	XP_016865453.1:p.Pro4663Ala
XM_017009965.1:c.13987C>G	XP_016865454.1:p.Pro4663Ala
XM_017009966.2:c.13909C>G	XP_016865455.1:p.Pro4637Ala
XM_017009967.1:c.13894C>G	XP_016865456.1:p.Pro4632Ala
XM_017009968.2:c.13990C>G	XP_016865457.1:p.Pro4664Ala
XM_017009969.2:c.13990C>G	XP_016865458.1:p.Pro4664Ala
XM_017009970.2:c.13990C>G	XP_016865459.1:p.Pro4664Ala
XM_017009971.2:c.13990C>G	XP_016865460.1:p.Pro4664Ala
XM_017009972.1:c.7108C>G	XP_016865461.1:p.Pro2370Ala
XM_017009973.1:c.7087C>G	XP_016865462.1:p.Pro2363Ala
NR_003149.2:n.13985C>G