Canonical Allele Identifier: CA360366891

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050914C>G (hg19) ; chr5:g.90755097C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755097C>G , CM000667.2:g.90755097C>G	GRCh38
NC_000005.9:g.90050914C>G , CM000667.1:g.90050914C>G	GRCh37
NC_000005.8:g.90086670C>G	NCBI36
NG_007083.1:g.201298C>G
NG_007083.2:g.230754C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11492C>G MANE Select	ENSP00000384582.2:p.Thr3831Ser
ENST00000425867.3:c.623C>G	ENSP00000392618.3:p.Thr208Ser
ENST00000639431.1:c.265+78888C>G	ENSP00000491057.1:n.265+78888C>G
ENST00000640374.1:n.4636C>G
ENST00000640464.1:n.1911C>G
ENST00000405460.6:c.11492C>G	ENSP00000384582.2:p.Thr3831Ser
ENST00000509621.1:c.4189C>G
NM_032119.3:c.11492C>G	NP_115495.3:p.Thr3831Ser
NR_003149.1:n.11505C>G
XM_011543675.1:c.11489C>G	XP_011541977.1:p.Thr3830Ser
XM_011543676.1:c.11411C>G	XP_011541978.1:p.Thr3804Ser
XM_011543677.1:c.8795C>G	XP_011541979.1:p.Thr2932Ser
XM_011543678.1:c.11492C>G	XP_011541980.1:p.Thr3831Ser
NM_032119.4:c.11492C>G MANE Select	NP_115495.3:p.Thr3831Ser
XM_017009963.2:c.11513C>G	XP_016865452.1:p.Thr3838Ser
XM_017009964.2:c.11510C>G	XP_016865453.1:p.Thr3837Ser
XM_017009965.1:c.11510C>G	XP_016865454.1:p.Thr3837Ser
XM_017009966.2:c.11432C>G	XP_016865455.1:p.Thr3811Ser
XM_017009967.1:c.11417C>G	XP_016865456.1:p.Thr3806Ser
XM_017009968.2:c.11513C>G	XP_016865457.1:p.Thr3838Ser
XM_017009969.2:c.11513C>G	XP_016865458.1:p.Thr3838Ser
XM_017009970.2:c.11513C>G	XP_016865459.1:p.Thr3838Ser
XM_017009971.2:c.11513C>G	XP_016865460.1:p.Thr3838Ser
XM_017009972.1:c.4631C>G	XP_016865461.1:p.Thr1544Ser
XM_017009973.1:c.4610C>G	XP_016865462.1:p.Thr1537Ser
NR_003149.2:n.11508C>G