Canonical Allele Identifier: CA360372126

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90757159C>T , CM000667.2:g.90757159C>T	GRCh38
NC_000005.9:g.90052976C>T , CM000667.1:g.90052976C>T	GRCh37
NC_000005.8:g.90088732C>T	NCBI36
NG_007083.1:g.203360C>T
NG_007083.2:g.232816C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11938C>T MANE Select	NP_115495.3:p.Gln3980Ter
ENST00000405460.9:c.11938C>T MANE Select	ENSP00000384582.2:p.Gln3980Ter
NM_032119.3:c.11938C>T	NP_115495.3:p.Gln3980Ter
NR_003149.1:n.11951C>T
NR_003149.2:n.11954C>T
ENST00000405460.6:c.11938C>T	ENSP00000384582.2:p.Gln3980Ter
ENST00000425867.3:c.892C>T	ENSP00000392618.3:p.Gln298Ter
ENST00000509621.1:c.4635C>T
ENST00000639431.1:c.265+80950C>T	ENSP00000491057.1:n.265+80950C>T
ENST00000639884.1:n.592C>T
ENST00000640374.1:n.4905C>T
ENST00000640464.1:n.2357C>T
XM_011543675.1:c.11935C>T	XP_011541977.1:p.Gln3979Ter
XM_011543676.1:c.11857C>T	XP_011541978.1:p.Gln3953Ter
XM_011543677.1:c.9241C>T	XP_011541979.1:p.Gln3081Ter
XM_011543678.1:c.11938C>T	XP_011541980.1:p.Gln3980Ter
XM_017009963.2:c.11959C>T	XP_016865452.1:p.Gln3987Ter
XM_017009964.2:c.11956C>T	XP_016865453.1:p.Gln3986Ter
XM_017009965.1:c.11956C>T	XP_016865454.1:p.Gln3986Ter
XM_017009966.2:c.11878C>T	XP_016865455.1:p.Gln3960Ter
XM_017009967.1:c.11863C>T	XP_016865456.1:p.Gln3955Ter
XM_017009968.2:c.11959C>T	XP_016865457.1:p.Gln3987Ter
XM_017009969.2:c.11959C>T	XP_016865458.1:p.Gln3987Ter
XM_017009970.2:c.11959C>T	XP_016865459.1:p.Gln3987Ter
XM_017009971.2:c.11959C>T	XP_016865460.1:p.Gln3987Ter
XM_017009972.1:c.5077C>T	XP_016865461.1:p.Gln1693Ter
XM_017009973.1:c.5056C>T	XP_016865462.1:p.Gln1686Ter