Canonical Allele Identifier: CA3341053

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90756981C>T , CM000667.2:g.90756981C>T	GRCh38
NC_000005.9:g.90052798C>T , CM000667.1:g.90052798C>T	GRCh37
NC_000005.8:g.90088554C>T	NCBI36
NG_007083.1:g.203182C>T
NG_007083.2:g.232638C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11760C>T MANE Select	NP_115495.3:p.Gly3920=
ENST00000405460.9:c.11760C>T MANE Select	ENSP00000384582.2:p.Gly3920=
NM_032119.3:c.11760C>T	NP_115495.3:p.Gly3920=
NR_003149.1:n.11773C>T
NR_003149.2:n.11776C>T
ENST00000405460.6:c.11760C>T	ENSP00000384582.2:p.Gly3920=
ENST00000425867.3:c.714C>T	ENSP00000392618.3:p.Gly238=
ENST00000509621.1:c.4457C>T
ENST00000639431.1:c.265+80772C>T	ENSP00000491057.1:n.265+80772C>T
ENST00000639884.1:n.414C>T
ENST00000640374.1:n.4727C>T
ENST00000640464.1:n.2179C>T
XM_011543675.1:c.11757C>T	XP_011541977.1:p.Gly3919=
XM_011543676.1:c.11679C>T	XP_011541978.1:p.Gly3893=
XM_011543677.1:c.9063C>T	XP_011541979.1:p.Gly3021=
XM_011543678.1:c.11760C>T	XP_011541980.1:p.Gly3920=
XM_017009963.2:c.11781C>T	XP_016865452.1:p.Gly3927=
XM_017009964.2:c.11778C>T	XP_016865453.1:p.Gly3926=
XM_017009965.1:c.11778C>T	XP_016865454.1:p.Gly3926=
XM_017009966.2:c.11700C>T	XP_016865455.1:p.Gly3900=
XM_017009967.1:c.11685C>T	XP_016865456.1:p.Gly3895=
XM_017009968.2:c.11781C>T	XP_016865457.1:p.Gly3927=
XM_017009969.2:c.11781C>T	XP_016865458.1:p.Gly3927=
XM_017009970.2:c.11781C>T	XP_016865459.1:p.Gly3927=
XM_017009971.2:c.11781C>T	XP_016865460.1:p.Gly3927=
XM_017009972.1:c.4899C>T	XP_016865461.1:p.Gly1633=
XM_017009973.1:c.4878C>T	XP_016865462.1:p.Gly1626=