Canonical Allele Identifier: CA445416022

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041414T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745597T>C , CM000667.2:g.90745597T>C	GRCh38
NC_000005.9:g.90041414T>C , CM000667.1:g.90041414T>C	GRCh37
NC_000005.8:g.90077170T>C	NCBI36
NG_007083.1:g.191798T>C
NG_007083.2:g.221254T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10776T>C MANE Select	ENSP00000384582.2:p.Gly3592=
ENST00000639431.1:c.265+69388T>C	ENSP00000491057.1:n.265+69388T>C
ENST00000640374.1:n.3920T>C
ENST00000640464.1:n.1195T>C
ENST00000405460.6:c.10776T>C	ENSP00000384582.2:p.Gly3592=
ENST00000509621.1:c.3473T>C
NM_032119.3:c.10776T>C	NP_115495.3:p.Gly3592=
NR_003149.1:n.10789T>C
XM_011543675.1:c.10773T>C	XP_011541977.1:p.Gly3591=
XM_011543676.1:c.10695T>C	XP_011541978.1:p.Gly3565=
XM_011543677.1:c.8079T>C	XP_011541979.1:p.Gly2693=
XM_011543678.1:c.10776T>C	XP_011541980.1:p.Gly3592=
XM_011543679.1:c.10771T>C	XP_011541981.1:p.Ter3591Arg
NM_032119.4:c.10776T>C MANE Select	NP_115495.3:p.Gly3592=
XM_017009963.2:c.10797T>C	XP_016865452.1:p.Gly3599=
XM_017009964.2:c.10794T>C	XP_016865453.1:p.Gly3598=
XM_017009965.1:c.10794T>C	XP_016865454.1:p.Gly3598=
XM_017009966.2:c.10716T>C	XP_016865455.1:p.Gly3572=
XM_017009967.1:c.10701T>C	XP_016865456.1:p.Gly3567=
XM_017009968.2:c.10797T>C	XP_016865457.1:p.Gly3599=
XM_017009969.2:c.10797T>C	XP_016865458.1:p.Gly3599=
XM_017009970.2:c.10797T>C	XP_016865459.1:p.Gly3599=
XM_017009971.2:c.10797T>C	XP_016865460.1:p.Gly3599=
XM_017009972.1:c.3915T>C	XP_016865461.1:p.Gly1305=
XM_017009973.1:c.3894T>C	XP_016865462.1:p.Gly1298=
XM_017009974.2:c.10792T>C	XP_016865463.1:p.Ter3598Arg
NR_003149.2:n.10792T>C