Canonical Allele Identifier: CA360366747

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050895C>T (hg19) ; chr5:g.90755078C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755078C>T , CM000667.2:g.90755078C>T	GRCh38
NC_000005.9:g.90050895C>T , CM000667.1:g.90050895C>T	GRCh37
NC_000005.8:g.90086651C>T	NCBI36
NG_007083.1:g.201279C>T
NG_007083.2:g.230735C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11473C>T MANE Select	ENSP00000384582.2:p.His3825Tyr
ENST00000425867.3:c.604C>T	ENSP00000392618.3:p.His202Tyr
ENST00000639431.1:c.265+78869C>T	ENSP00000491057.1:n.265+78869C>T
ENST00000640374.1:n.4617C>T
ENST00000640464.1:n.1892C>T
ENST00000405460.6:c.11473C>T	ENSP00000384582.2:p.His3825Tyr
ENST00000509621.1:c.4170C>T
NM_032119.3:c.11473C>T	NP_115495.3:p.His3825Tyr
NR_003149.1:n.11486C>T
XM_011543675.1:c.11470C>T	XP_011541977.1:p.His3824Tyr
XM_011543676.1:c.11392C>T	XP_011541978.1:p.His3798Tyr
XM_011543677.1:c.8776C>T	XP_011541979.1:p.His2926Tyr
XM_011543678.1:c.11473C>T	XP_011541980.1:p.His3825Tyr
NM_032119.4:c.11473C>T MANE Select	NP_115495.3:p.His3825Tyr
XM_017009963.2:c.11494C>T	XP_016865452.1:p.His3832Tyr
XM_017009964.2:c.11491C>T	XP_016865453.1:p.His3831Tyr
XM_017009965.1:c.11491C>T	XP_016865454.1:p.His3831Tyr
XM_017009966.2:c.11413C>T	XP_016865455.1:p.His3805Tyr
XM_017009967.1:c.11398C>T	XP_016865456.1:p.His3800Tyr
XM_017009968.2:c.11494C>T	XP_016865457.1:p.His3832Tyr
XM_017009969.2:c.11494C>T	XP_016865458.1:p.His3832Tyr
XM_017009970.2:c.11494C>T	XP_016865459.1:p.His3832Tyr
XM_017009971.2:c.11494C>T	XP_016865460.1:p.His3832Tyr
XM_017009972.1:c.4612C>T	XP_016865461.1:p.His1538Tyr
XM_017009973.1:c.4591C>T	XP_016865462.1:p.His1531Tyr
NR_003149.2:n.11489C>T