Canonical Allele Identifier: CA445404212

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050978T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755161T>C , CM000667.2:g.90755161T>C	GRCh38
NC_000005.9:g.90050978T>C , CM000667.1:g.90050978T>C	GRCh37
NC_000005.8:g.90086734T>C	NCBI36
NG_007083.1:g.201362T>C
NG_007083.2:g.230818T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11556T>C MANE Select	ENSP00000384582.2:p.Ala3852=
ENST00000425867.3:c.687T>C	ENSP00000392618.3:p.Ala229=
ENST00000639431.1:c.265+78952T>C	ENSP00000491057.1:n.265+78952T>C
ENST00000640374.1:n.4700T>C
ENST00000640464.1:n.1975T>C
ENST00000405460.6:c.11556T>C	ENSP00000384582.2:p.Ala3852=
ENST00000509621.1:c.4253T>C
NM_032119.3:c.11556T>C	NP_115495.3:p.Ala3852=
NR_003149.1:n.11569T>C
XM_011543675.1:c.11553T>C	XP_011541977.1:p.Ala3851=
XM_011543676.1:c.11475T>C	XP_011541978.1:p.Ala3825=
XM_011543677.1:c.8859T>C	XP_011541979.1:p.Ala2953=
XM_011543678.1:c.11556T>C	XP_011541980.1:p.Ala3852=
NM_032119.4:c.11556T>C MANE Select	NP_115495.3:p.Ala3852=
XM_017009963.2:c.11577T>C	XP_016865452.1:p.Ala3859=
XM_017009964.2:c.11574T>C	XP_016865453.1:p.Ala3858=
XM_017009965.1:c.11574T>C	XP_016865454.1:p.Ala3858=
XM_017009966.2:c.11496T>C	XP_016865455.1:p.Ala3832=
XM_017009967.1:c.11481T>C	XP_016865456.1:p.Ala3827=
XM_017009968.2:c.11577T>C	XP_016865457.1:p.Ala3859=
XM_017009969.2:c.11577T>C	XP_016865458.1:p.Ala3859=
XM_017009970.2:c.11577T>C	XP_016865459.1:p.Ala3859=
XM_017009971.2:c.11577T>C	XP_016865460.1:p.Ala3859=
XM_017009972.1:c.4695T>C	XP_016865461.1:p.Ala1565=
XM_017009973.1:c.4674T>C	XP_016865462.1:p.Ala1558=
NR_003149.2:n.11572T>C