Canonical Allele Identifier: CA360366626

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050874G>T (hg19) ; chr5:g.90755057G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755057G>T , CM000667.2:g.90755057G>T	GRCh38
NC_000005.9:g.90050874G>T , CM000667.1:g.90050874G>T	GRCh37
NC_000005.8:g.90086630G>T	NCBI36
NG_007083.1:g.201258G>T
NG_007083.2:g.230714G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11452G>T MANE Select	ENSP00000384582.2:p.Ala3818Ser
ENST00000425867.3:c.583G>T	ENSP00000392618.3:p.Ala195Ser
ENST00000639431.1:c.265+78848G>T	ENSP00000491057.1:n.265+78848G>T
ENST00000640374.1:n.4596G>T
ENST00000640464.1:n.1871G>T
ENST00000405460.6:c.11452G>T	ENSP00000384582.2:p.Ala3818Ser
ENST00000509621.1:c.4149G>T
NM_032119.3:c.11452G>T	NP_115495.3:p.Ala3818Ser
NR_003149.1:n.11465G>T
XM_011543675.1:c.11449G>T	XP_011541977.1:p.Ala3817Ser
XM_011543676.1:c.11371G>T	XP_011541978.1:p.Ala3791Ser
XM_011543677.1:c.8755G>T	XP_011541979.1:p.Ala2919Ser
XM_011543678.1:c.11452G>T	XP_011541980.1:p.Ala3818Ser
NM_032119.4:c.11452G>T MANE Select	NP_115495.3:p.Ala3818Ser
XM_017009963.2:c.11473G>T	XP_016865452.1:p.Ala3825Ser
XM_017009964.2:c.11470G>T	XP_016865453.1:p.Ala3824Ser
XM_017009965.1:c.11470G>T	XP_016865454.1:p.Ala3824Ser
XM_017009966.2:c.11392G>T	XP_016865455.1:p.Ala3798Ser
XM_017009967.1:c.11377G>T	XP_016865456.1:p.Ala3793Ser
XM_017009968.2:c.11473G>T	XP_016865457.1:p.Ala3825Ser
XM_017009969.2:c.11473G>T	XP_016865458.1:p.Ala3825Ser
XM_017009970.2:c.11473G>T	XP_016865459.1:p.Ala3825Ser
XM_017009971.2:c.11473G>T	XP_016865460.1:p.Ala3825Ser
XM_017009972.1:c.4591G>T	XP_016865461.1:p.Ala1531Ser
XM_017009973.1:c.4570G>T	XP_016865462.1:p.Ala1524Ser
NR_003149.2:n.11468G>T