Canonical Allele Identifier: CA3341438

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90781418T>A , CM000667.2:g.90781418T>A	GRCh38
NC_000005.9:g.90077235T>A , CM000667.1:g.90077235T>A	GRCh37
NC_000005.8:g.90112991T>A	NCBI36
NG_007083.1:g.227619T>A
NG_007083.2:g.257075T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13083-12T>A MANE Select	NP_115495.3:n.13083-12T>A
ENST00000405460.9:c.13083-12T>A MANE Select	ENSP00000384582.2:n.13083-12T>A
NM_032119.3:c.13083-12T>A	NP_115495.3:n.13083-12T>A
NR_003149.1:n.13096-12T>A
NR_003149.2:n.13099-12T>A
ENST00000405460.6:c.13083-12T>A	ENSP00000384582.2:n.13083-12T>A
ENST00000425867.2:c.54T>A	ENSP00000392618.2:p.Tyr18Ter
ENST00000425867.3:c.2037-12T>A	ENSP00000392618.3:n.2037-12T>A
ENST00000638510.1:n.338T>A
ENST00000639431.1:c.265+105209T>A	ENSP00000491057.1:n.265+105209T>A
XM_011543675.1:c.13080-12T>A	XP_011541977.1:n.13080-12T>A
XM_011543676.1:c.13002-12T>A	XP_011541978.1:n.13002-12T>A
XM_011543677.1:c.10386-12T>A	XP_011541979.1:n.10386-12T>A
XM_011543678.1:c.13083-12T>A	XP_011541980.1:n.13083-12T>A
XM_017009963.2:c.13104-12T>A	XP_016865452.1:n.13104-12T>A
XM_017009964.2:c.13101-12T>A	XP_016865453.1:n.13101-12T>A
XM_017009965.1:c.13101-12T>A	XP_016865454.1:n.13101-12T>A
XM_017009966.2:c.13023-12T>A	XP_016865455.1:n.13023-12T>A
XM_017009967.1:c.13008-12T>A	XP_016865456.1:n.13008-12T>A
XM_017009968.2:c.13104-12T>A	XP_016865457.1:n.13104-12T>A
XM_017009969.2:c.13104-12T>A	XP_016865458.1:n.13104-12T>A
XM_017009970.2:c.13104-12T>A	XP_016865459.1:n.13104-12T>A
XM_017009971.2:c.13104-12T>A	XP_016865460.1:n.13104-12T>A
XM_017009972.1:c.6222-12T>A	XP_016865461.1:n.6222-12T>A
XM_017009973.1:c.6201-12T>A	XP_016865462.1:n.6201-12T>A