Canonical Allele Identifier: CA445467618

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90791214-A-G
• MyVariant Identifiers: chr5:g.90087031A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791214A>G , CM000667.2:g.90791214A>G	GRCh38
NC_000005.9:g.90087031A>G , CM000667.1:g.90087031A>G	GRCh37
NC_000005.8:g.90122787A>G	NCBI36
NG_007083.1:g.237415A>G
NG_007083.2:g.266871A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14385A>G MANE Select	ENSP00000384582.2:p.Gly4795=
ENST00000425867.3:c.3339A>G	ENSP00000392618.3:p.Gly1113=
ENST00000507314.2:c.60A>G	ENSP00000491299.1:p.Gly20=
ENST00000638510.1:n.1652A>G
ENST00000638585.1:n.151A>G
ENST00000638975.1:c.1014A>G	ENSP00000492630.1:p.Gly338=
ENST00000639431.1:c.265+115005A>G	ENSP00000491057.1:n.265+115005A>G
ENST00000640407.1:c.795A>G	ENSP00000491425.1:p.Gly265=
ENST00000405460.6:c.14385A>G	ENSP00000384582.2:p.Gly4795=
ENST00000425867.2:c.1368A>G	ENSP00000392618.2:p.Gly456=
ENST00000507314.1:n.60A>G
NM_032119.3:c.14385A>G	NP_115495.3:p.Gly4795=
NR_003149.1:n.14398A>G
XM_011543675.1:c.14382A>G	XP_011541977.1:p.Gly4794=
XM_011543676.1:c.14304A>G	XP_011541978.1:p.Gly4768=
XM_011543677.1:c.11688A>G	XP_011541979.1:p.Gly3896=
XM_011543678.1:c.14385A>G	XP_011541980.1:p.Gly4795=
NM_032119.4:c.14385A>G MANE Select	NP_115495.3:p.Gly4795=
XM_017009963.2:c.14406A>G	XP_016865452.1:p.Gly4802=
XM_017009964.2:c.14403A>G	XP_016865453.1:p.Gly4801=
XM_017009965.1:c.14403A>G	XP_016865454.1:p.Gly4801=
XM_017009966.2:c.14325A>G	XP_016865455.1:p.Gly4775=
XM_017009967.1:c.14310A>G	XP_016865456.1:p.Gly4770=
XM_017009968.2:c.14406A>G	XP_016865457.1:p.Gly4802=
XM_017009969.2:c.14406A>G	XP_016865458.1:p.Gly4802=
XM_017009970.2:c.14406A>G	XP_016865459.1:p.Gly4802=
XM_017009971.2:c.14406A>G	XP_016865460.1:p.Gly4802=
XM_017009972.1:c.7524A>G	XP_016865461.1:p.Gly2508=
XM_017009973.1:c.7503A>G	XP_016865462.1:p.Gly2501=
NR_003149.2:n.14401A>G