Canonical Allele Identifier: CA360401792

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791233C>T , CM000667.2:g.90791233C>T	GRCh38
NC_000005.9:g.90087050C>T , CM000667.1:g.90087050C>T	GRCh37
NC_000005.8:g.90122806C>T	NCBI36
NG_007083.1:g.237434C>T
NG_007083.2:g.266890C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14404C>T MANE Select	NP_115495.3:p.Arg4802Ter
ENST00000405460.9:c.14404C>T MANE Select	ENSP00000384582.2:p.Arg4802Ter
NM_032119.3:c.14404C>T	NP_115495.3:p.Arg4802Ter
NR_003149.1:n.14417C>T
NR_003149.2:n.14420C>T
ENST00000405460.6:c.14404C>T	ENSP00000384582.2:p.Arg4802Ter
ENST00000425867.2:c.1387C>T	ENSP00000392618.2:p.Arg463Ter
ENST00000425867.3:c.3358C>T	ENSP00000392618.3:p.Arg1120Ter
ENST00000507314.1:n.79C>T
ENST00000507314.2:c.79C>T	ENSP00000491299.1:p.Arg27Ter
ENST00000638510.1:n.1671C>T
ENST00000638585.1:n.170C>T
ENST00000638975.1:c.1033C>T	ENSP00000492630.1:p.Arg345Ter
ENST00000639431.1:c.265+115024C>T	ENSP00000491057.1:n.265+115024C>T
ENST00000640407.1:c.814C>T	ENSP00000491425.1:p.Arg272Ter
XM_011543675.1:c.14401C>T	XP_011541977.1:p.Arg4801Ter
XM_011543676.1:c.14323C>T	XP_011541978.1:p.Arg4775Ter
XM_011543677.1:c.11707C>T	XP_011541979.1:p.Arg3903Ter
XM_011543678.1:c.14404C>T	XP_011541980.1:p.Arg4802Ter
XM_017009963.2:c.14425C>T	XP_016865452.1:p.Arg4809Ter
XM_017009964.2:c.14422C>T	XP_016865453.1:p.Arg4808Ter
XM_017009965.1:c.14422C>T	XP_016865454.1:p.Arg4808Ter
XM_017009966.2:c.14344C>T	XP_016865455.1:p.Arg4782Ter
XM_017009967.1:c.14329C>T	XP_016865456.1:p.Arg4777Ter
XM_017009968.2:c.14425C>T	XP_016865457.1:p.Arg4809Ter
XM_017009969.2:c.14425C>T	XP_016865458.1:p.Arg4809Ter
XM_017009970.2:c.14425C>T	XP_016865459.1:p.Arg4809Ter
XM_017009971.2:c.14425C>T	XP_016865460.1:p.Arg4809Ter
XM_017009972.1:c.7543C>T	XP_016865461.1:p.Arg2515Ter
XM_017009973.1:c.7522C>T	XP_016865462.1:p.Arg2508Ter