Canonical Allele Identifier: CA445415213

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729655A>T , CM000667.2:g.90729655A>T	GRCh38
NC_000005.9:g.90025472A>T , CM000667.1:g.90025472A>T	GRCh37
NC_000005.8:g.90061228A>T	NCBI36
NG_007083.1:g.175856A>T
NG_007083.2:g.205312A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10440A>T MANE Select	NP_115495.3:p.Ser3480=
ENST00000405460.9:c.10440A>T MANE Select	ENSP00000384582.2:p.Ser3480=
NM_032119.3:c.10440A>T	NP_115495.3:p.Ser3480=
NR_003149.1:n.10453A>T
NR_003149.2:n.10456A>T
ENST00000405460.6:c.10440A>T	ENSP00000384582.2:p.Ser3480=
ENST00000509621.1:c.3137A>T
ENST00000639431.1:c.265+53446A>T	ENSP00000491057.1:n.265+53446A>T
ENST00000640374.1:n.3584A>T
ENST00000640464.1:n.859A>T
XM_011543675.1:c.10437A>T	XP_011541977.1:p.Ser3479=
XM_011543676.1:c.10359A>T	XP_011541978.1:p.Ser3453=
XM_011543677.1:c.7743A>T	XP_011541979.1:p.Ser2581=
XM_011543678.1:c.10440A>T	XP_011541980.1:p.Ser3480=
XM_011543679.1:c.10440A>T	XP_011541981.1:p.Ser3480=
XM_017009963.2:c.10461A>T	XP_016865452.1:p.Ser3487=
XM_017009964.2:c.10458A>T	XP_016865453.1:p.Ser3486=
XM_017009965.1:c.10458A>T	XP_016865454.1:p.Ser3486=
XM_017009966.2:c.10380A>T	XP_016865455.1:p.Ser3460=
XM_017009967.1:c.10365A>T	XP_016865456.1:p.Ser3455=
XM_017009968.2:c.10461A>T	XP_016865457.1:p.Ser3487=
XM_017009969.2:c.10461A>T	XP_016865458.1:p.Ser3487=
XM_017009970.2:c.10461A>T	XP_016865459.1:p.Ser3487=
XM_017009971.2:c.10461A>T	XP_016865460.1:p.Ser3487=
XM_017009972.1:c.3579A>T	XP_016865461.1:p.Ser1193=
XM_017009973.1:c.3558A>T	XP_016865462.1:p.Ser1186=
XM_017009974.2:c.10461A>T	XP_016865463.1:p.Ser3487=
XR_001742802.1:n.2522+11252T>A
XR_948560.1:n.271+11252T>A