Canonical Allele Identifier: CA3341332

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90778546C>T , CM000667.2:g.90778546C>T	GRCh38
NC_000005.9:g.90074363C>T , CM000667.1:g.90074363C>T	GRCh37
NC_000005.8:g.90110119C>T	NCBI36
NG_007083.1:g.224747C>T
NG_007083.2:g.254203C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12786C>T MANE Select	NP_115495.3:p.Ser4262=
ENST00000405460.9:c.12786C>T MANE Select	ENSP00000384582.2:p.Ser4262=
NM_032119.3:c.12786C>T	NP_115495.3:p.Ser4262=
NR_003149.1:n.12799C>T
NR_003149.2:n.12802C>T
ENST00000405460.6:c.12786C>T	ENSP00000384582.2:p.Ser4262=
ENST00000425867.3:c.1740C>T	ENSP00000392618.3:p.Ser580=
ENST00000639431.1:c.265+102337C>T	ENSP00000491057.1:n.265+102337C>T
ENST00000640464.1:n.3205C>T
XM_011543675.1:c.12783C>T	XP_011541977.1:p.Ser4261=
XM_011543676.1:c.12705C>T	XP_011541978.1:p.Ser4235=
XM_011543677.1:c.10089C>T	XP_011541979.1:p.Ser3363=
XM_011543678.1:c.12786C>T	XP_011541980.1:p.Ser4262=
XM_017009963.2:c.12807C>T	XP_016865452.1:p.Ser4269=
XM_017009964.2:c.12804C>T	XP_016865453.1:p.Ser4268=
XM_017009965.1:c.12804C>T	XP_016865454.1:p.Ser4268=
XM_017009966.2:c.12726C>T	XP_016865455.1:p.Ser4242=
XM_017009967.1:c.12711C>T	XP_016865456.1:p.Ser4237=
XM_017009968.2:c.12807C>T	XP_016865457.1:p.Ser4269=
XM_017009969.2:c.12807C>T	XP_016865458.1:p.Ser4269=
XM_017009970.2:c.12807C>T	XP_016865459.1:p.Ser4269=
XM_017009971.2:c.12807C>T	XP_016865460.1:p.Ser4269=
XM_017009972.1:c.5925C>T	XP_016865461.1:p.Ser1975=
XM_017009973.1:c.5904C>T	XP_016865462.1:p.Ser1968=