Canonical Allele Identifier: CA3341463

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90781574C>T , CM000667.2:g.90781574C>T	GRCh38
NC_000005.9:g.90077391C>T , CM000667.1:g.90077391C>T	GRCh37
NC_000005.8:g.90113147C>T	NCBI36
NG_007083.1:g.227775C>T
NG_007083.2:g.257231C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13227C>T MANE Select	NP_115495.3:p.Phe4409=
ENST00000405460.9:c.13227C>T MANE Select	ENSP00000384582.2:p.Phe4409=
NM_032119.3:c.13227C>T	NP_115495.3:p.Phe4409=
NR_003149.1:n.13240C>T
NR_003149.2:n.13243C>T
ENST00000405460.6:c.13227C>T	ENSP00000384582.2:p.Phe4409=
ENST00000425867.2:c.210C>T	ENSP00000392618.2:p.Phe70=
ENST00000425867.3:c.2181C>T	ENSP00000392618.3:p.Phe727=
ENST00000638510.1:n.494C>T
ENST00000639431.1:c.265+105365C>T	ENSP00000491057.1:n.265+105365C>T
XM_011543675.1:c.13224C>T	XP_011541977.1:p.Phe4408=
XM_011543676.1:c.13146C>T	XP_011541978.1:p.Phe4382=
XM_011543677.1:c.10530C>T	XP_011541979.1:p.Phe3510=
XM_011543678.1:c.13227C>T	XP_011541980.1:p.Phe4409=
XM_017009963.2:c.13248C>T	XP_016865452.1:p.Phe4416=
XM_017009964.2:c.13245C>T	XP_016865453.1:p.Phe4415=
XM_017009965.1:c.13245C>T	XP_016865454.1:p.Phe4415=
XM_017009966.2:c.13167C>T	XP_016865455.1:p.Phe4389=
XM_017009967.1:c.13152C>T	XP_016865456.1:p.Phe4384=
XM_017009968.2:c.13248C>T	XP_016865457.1:p.Phe4416=
XM_017009969.2:c.13248C>T	XP_016865458.1:p.Phe4416=
XM_017009970.2:c.13248C>T	XP_016865459.1:p.Phe4416=
XM_017009971.2:c.13248C>T	XP_016865460.1:p.Phe4416=
XM_017009972.1:c.6366C>T	XP_016865461.1:p.Phe2122=
XM_017009973.1:c.6345C>T	XP_016865462.1:p.Phe2115=