Canonical Allele Identifier: CA360429147

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985395C>T , CM000667.2:g.90985395C>T	GRCh38
NC_000005.9:g.90281212C>T , CM000667.1:g.90281212C>T	GRCh37
NC_000005.8:g.90316968C>T	NCBI36
NG_007083.1:g.431596C>T
NG_007083.2:g.461052C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18025C>T MANE Select	NP_115495.3:p.Arg6009Ter
ENST00000405460.9:c.18025C>T MANE Select	ENSP00000384582.2:p.Arg6009Ter
NM_032119.3:c.18025C>T	NP_115495.3:p.Arg6009Ter
NR_003149.1:n.18038C>T
NR_003149.2:n.18041C>T
ENST00000405460.6:c.18025C>T	ENSP00000384582.2:p.Arg6009Ter
ENST00000425867.2:c.5008C>T	ENSP00000392618.2:p.Arg1670Ter
ENST00000425867.3:c.6979C>T	ENSP00000392618.3:p.Arg2327Ter
ENST00000638510.1:n.5292C>T
ENST00000638990.1:c.1237C>T
ENST00000639431.1:c.317C>T	ENSP00000491057.1:n.317C>T
ENST00000639707.1:c.109C>T	ENSP00000492328.1:p.Arg37Ter
ENST00000639821.1:c.109C>T	ENSP00000492216.1:p.Arg37Ter
ENST00000640369.1:c.109C>T	ENSP00000491401.1:p.Arg37Ter
ENST00000640407.1:c.4474C>T	ENSP00000491425.1:n.4474C>T
ENST00000640815.1:c.109C>T	ENSP00000491767.1:p.Arg37Ter
XM_011543675.1:c.18022C>T	XP_011541977.1:p.Arg6008Ter
XM_011543676.1:c.17944C>T	XP_011541978.1:p.Arg5982Ter
XM_011543677.1:c.15328C>T	XP_011541979.1:p.Arg5110Ter
XM_017009963.2:c.18046C>T	XP_016865452.1:p.Arg6016Ter
XM_017009964.2:c.18043C>T	XP_016865453.1:p.Arg6015Ter
XM_017009965.1:c.18043C>T	XP_016865454.1:p.Arg6015Ter
XM_017009966.2:c.17965C>T	XP_016865455.1:p.Arg5989Ter
XM_017009967.1:c.17950C>T	XP_016865456.1:p.Arg5984Ter
XM_017009968.2:c.17866C>T	XP_016865457.1:p.Arg5956Ter
XM_017009969.2:c.18046C>T	XP_016865458.1:p.Arg6016Ter
XM_017009972.1:c.11164C>T	XP_016865461.1:p.Arg3722Ter
XM_017009973.1:c.11143C>T	XP_016865462.1:p.Arg3715Ter