Canonical Allele Identifier: CA360369505

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90756556G>T , CM000667.2:g.90756556G>T	GRCh38
NC_000005.9:g.90052373G>T , CM000667.1:g.90052373G>T	GRCh37
NC_000005.8:g.90088129G>T	NCBI36
NG_007083.1:g.202757G>T
NG_007083.2:g.232213G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11683G>T MANE Select	NP_115495.3:p.Gly3895Ter
ENST00000405460.9:c.11683G>T MANE Select	ENSP00000384582.2:p.Gly3895Ter
NM_032119.3:c.11683G>T	NP_115495.3:p.Gly3895Ter
NR_003149.1:n.11696G>T
NR_003149.2:n.11699G>T
ENST00000405460.6:c.11683G>T	ENSP00000384582.2:p.Gly3895Ter
ENST00000425867.3:c.712-423G>T	ENSP00000392618.3:n.712-423G>T
ENST00000509621.1:c.4380G>T
ENST00000639431.1:c.265+80347G>T	ENSP00000491057.1:n.265+80347G>T
ENST00000640374.1:n.4725-423G>T
ENST00000640464.1:n.2102G>T
XM_011543675.1:c.11680G>T	XP_011541977.1:p.Gly3894Ter
XM_011543676.1:c.11602G>T	XP_011541978.1:p.Gly3868Ter
XM_011543677.1:c.8986G>T	XP_011541979.1:p.Gly2996Ter
XM_011543678.1:c.11683G>T	XP_011541980.1:p.Gly3895Ter
XM_017009963.2:c.11704G>T	XP_016865452.1:p.Gly3902Ter
XM_017009964.2:c.11701G>T	XP_016865453.1:p.Gly3901Ter
XM_017009965.1:c.11701G>T	XP_016865454.1:p.Gly3901Ter
XM_017009966.2:c.11623G>T	XP_016865455.1:p.Gly3875Ter
XM_017009967.1:c.11608G>T	XP_016865456.1:p.Gly3870Ter
XM_017009968.2:c.11704G>T	XP_016865457.1:p.Gly3902Ter
XM_017009969.2:c.11704G>T	XP_016865458.1:p.Gly3902Ter
XM_017009970.2:c.11704G>T	XP_016865459.1:p.Gly3902Ter
XM_017009971.2:c.11704G>T	XP_016865460.1:p.Gly3902Ter
XM_017009972.1:c.4822G>T	XP_016865461.1:p.Gly1608Ter
XM_017009973.1:c.4801G>T	XP_016865462.1:p.Gly1601Ter