Canonical Allele Identifier: CA360367501

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90051000C>G (hg19) ; chr5:g.90755183C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755183C>G , CM000667.2:g.90755183C>G	GRCh38
NC_000005.9:g.90051000C>G , CM000667.1:g.90051000C>G	GRCh37
NC_000005.8:g.90086756C>G	NCBI36
NG_007083.1:g.201384C>G
NG_007083.2:g.230840C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11578C>G MANE Select	ENSP00000384582.2:p.Pro3860Ala
ENST00000425867.3:c.709C>G	ENSP00000392618.3:p.Pro237Ala
ENST00000639431.1:c.265+78974C>G	ENSP00000491057.1:n.265+78974C>G
ENST00000640374.1:n.4722C>G
ENST00000640464.1:n.1997C>G
ENST00000405460.6:c.11578C>G	ENSP00000384582.2:p.Pro3860Ala
ENST00000509621.1:c.4275C>G
NM_032119.3:c.11578C>G	NP_115495.3:p.Pro3860Ala
NR_003149.1:n.11591C>G
XM_011543675.1:c.11575C>G	XP_011541977.1:p.Pro3859Ala
XM_011543676.1:c.11497C>G	XP_011541978.1:p.Pro3833Ala
XM_011543677.1:c.8881C>G	XP_011541979.1:p.Pro2961Ala
XM_011543678.1:c.11578C>G	XP_011541980.1:p.Pro3860Ala
NM_032119.4:c.11578C>G MANE Select	NP_115495.3:p.Pro3860Ala
XM_017009963.2:c.11599C>G	XP_016865452.1:p.Pro3867Ala
XM_017009964.2:c.11596C>G	XP_016865453.1:p.Pro3866Ala
XM_017009965.1:c.11596C>G	XP_016865454.1:p.Pro3866Ala
XM_017009966.2:c.11518C>G	XP_016865455.1:p.Pro3840Ala
XM_017009967.1:c.11503C>G	XP_016865456.1:p.Pro3835Ala
XM_017009968.2:c.11599C>G	XP_016865457.1:p.Pro3867Ala
XM_017009969.2:c.11599C>G	XP_016865458.1:p.Pro3867Ala
XM_017009970.2:c.11599C>G	XP_016865459.1:p.Pro3867Ala
XM_017009971.2:c.11599C>G	XP_016865460.1:p.Pro3867Ala
XM_017009972.1:c.4717C>G	XP_016865461.1:p.Pro1573Ala
XM_017009973.1:c.4696C>G	XP_016865462.1:p.Pro1566Ala
NR_003149.2:n.11594C>G