Canonical Allele Identifier: CA3342088

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823453C>T , CM000667.2:g.90823453C>T	GRCh38
NC_000005.9:g.90119270C>T , CM000667.1:g.90119270C>T	GRCh37
NC_000005.8:g.90155026C>T	NCBI36
NG_007083.1:g.269654C>T
NG_007083.2:g.299110C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16225C>T MANE Select	NP_115495.3:p.Arg5409Ter
ENST00000405460.9:c.16225C>T MANE Select	ENSP00000384582.2:p.Arg5409Ter
NM_032119.3:c.16225C>T	NP_115495.3:p.Arg5409Ter
NR_003149.1:n.16238C>T
NR_003149.2:n.16241C>T
ENST00000405460.6:c.16225C>T	ENSP00000384582.2:p.Arg5409Ter
ENST00000425867.2:c.3208C>T	ENSP00000392618.2:p.Arg1070Ter
ENST00000425867.3:c.5179C>T	ENSP00000392618.3:p.Arg1727Ter
ENST00000638510.1:n.3492C>T
ENST00000639431.1:c.265+147244C>T	ENSP00000491057.1:n.265+147244C>T
ENST00000640061.1:n.128+1271C>T
ENST00000640407.1:c.2635C>T	ENSP00000491425.1:p.Arg879Ter
XM_011543675.1:c.16222C>T	XP_011541977.1:p.Arg5408Ter
XM_011543676.1:c.16144C>T	XP_011541978.1:p.Arg5382Ter
XM_011543677.1:c.13528C>T	XP_011541979.1:p.Arg4510Ter
XM_017009963.2:c.16246C>T	XP_016865452.1:p.Arg5416Ter
XM_017009964.2:c.16243C>T	XP_016865453.1:p.Arg5415Ter
XM_017009965.1:c.16243C>T	XP_016865454.1:p.Arg5415Ter
XM_017009966.2:c.16165C>T	XP_016865455.1:p.Arg5389Ter
XM_017009967.1:c.16150C>T	XP_016865456.1:p.Arg5384Ter
XM_017009968.2:c.16066C>T	XP_016865457.1:p.Arg5356Ter
XM_017009969.2:c.16246C>T	XP_016865458.1:p.Arg5416Ter
XM_017009972.1:c.9364C>T	XP_016865461.1:p.Arg3122Ter
XM_017009973.1:c.9343C>T	XP_016865462.1:p.Arg3115Ter