Canonical Allele Identifier: CA360378075

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763395C>T , CM000667.2:g.90763395C>T	GRCh38
NC_000005.9:g.90059212C>T , CM000667.1:g.90059212C>T	GRCh37
NC_000005.8:g.90094968C>T	NCBI36
NG_007083.1:g.209596C>T
NG_007083.2:g.239052C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12211C>T MANE Select	NP_115495.3:p.Arg4071Ter
ENST00000405460.9:c.12211C>T MANE Select	ENSP00000384582.2:p.Arg4071Ter
NM_032119.3:c.12211C>T	NP_115495.3:p.Arg4071Ter
NR_003149.1:n.12224C>T
NR_003149.2:n.12227C>T
ENST00000405460.6:c.12211C>T	ENSP00000384582.2:p.Arg4071Ter
ENST00000425867.3:c.1165C>T	ENSP00000392618.3:p.Arg389Ter
ENST00000639431.1:c.265+87186C>T	ENSP00000491057.1:n.265+87186C>T
ENST00000640464.1:n.2630C>T
ENST00000640729.1:n.788C>T
XM_011543675.1:c.12208C>T	XP_011541977.1:p.Arg4070Ter
XM_011543676.1:c.12130C>T	XP_011541978.1:p.Arg4044Ter
XM_011543677.1:c.9514C>T	XP_011541979.1:p.Arg3172Ter
XM_011543678.1:c.12211C>T	XP_011541980.1:p.Arg4071Ter
XM_017009963.2:c.12232C>T	XP_016865452.1:p.Arg4078Ter
XM_017009964.2:c.12229C>T	XP_016865453.1:p.Arg4077Ter
XM_017009965.1:c.12229C>T	XP_016865454.1:p.Arg4077Ter
XM_017009966.2:c.12151C>T	XP_016865455.1:p.Arg4051Ter
XM_017009967.1:c.12136C>T	XP_016865456.1:p.Arg4046Ter
XM_017009968.2:c.12232C>T	XP_016865457.1:p.Arg4078Ter
XM_017009969.2:c.12232C>T	XP_016865458.1:p.Arg4078Ter
XM_017009970.2:c.12232C>T	XP_016865459.1:p.Arg4078Ter
XM_017009971.2:c.12232C>T	XP_016865460.1:p.Arg4078Ter
XM_017009972.1:c.5350C>T	XP_016865461.1:p.Arg1784Ter
XM_017009973.1:c.5329C>T	XP_016865462.1:p.Arg1777Ter