Canonical Allele Identifier: CA360369965

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90756586G>T , CM000667.2:g.90756586G>T	GRCh38
NC_000005.9:g.90052403G>T , CM000667.1:g.90052403G>T	GRCh37
NC_000005.8:g.90088159G>T	NCBI36
NG_007083.1:g.202787G>T
NG_007083.2:g.232243G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11713G>T MANE Select	NP_115495.3:p.Glu3905Ter
ENST00000405460.9:c.11713G>T MANE Select	ENSP00000384582.2:p.Glu3905Ter
NM_032119.3:c.11713G>T	NP_115495.3:p.Glu3905Ter
NR_003149.1:n.11726G>T
NR_003149.2:n.11729G>T
ENST00000405460.6:c.11713G>T	ENSP00000384582.2:p.Glu3905Ter
ENST00000425867.3:c.712-393G>T	ENSP00000392618.3:n.712-393G>T
ENST00000509621.1:c.4410G>T
ENST00000639431.1:c.265+80377G>T	ENSP00000491057.1:n.265+80377G>T
ENST00000639884.1:n.19G>T
ENST00000640374.1:n.4725-393G>T
ENST00000640464.1:n.2132G>T
XM_011543675.1:c.11710G>T	XP_011541977.1:p.Glu3904Ter
XM_011543676.1:c.11632G>T	XP_011541978.1:p.Glu3878Ter
XM_011543677.1:c.9016G>T	XP_011541979.1:p.Glu3006Ter
XM_011543678.1:c.11713G>T	XP_011541980.1:p.Glu3905Ter
XM_017009963.2:c.11734G>T	XP_016865452.1:p.Glu3912Ter
XM_017009964.2:c.11731G>T	XP_016865453.1:p.Glu3911Ter
XM_017009965.1:c.11731G>T	XP_016865454.1:p.Glu3911Ter
XM_017009966.2:c.11653G>T	XP_016865455.1:p.Glu3885Ter
XM_017009967.1:c.11638G>T	XP_016865456.1:p.Glu3880Ter
XM_017009968.2:c.11734G>T	XP_016865457.1:p.Glu3912Ter
XM_017009969.2:c.11734G>T	XP_016865458.1:p.Glu3912Ter
XM_017009970.2:c.11734G>T	XP_016865459.1:p.Glu3912Ter
XM_017009971.2:c.11734G>T	XP_016865460.1:p.Glu3912Ter
XM_017009972.1:c.4852G>T	XP_016865461.1:p.Glu1618Ter
XM_017009973.1:c.4831G>T	XP_016865462.1:p.Glu1611Ter