Canonical Allele Identifier: CA360403009

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087163G>T (hg19) ; chr5:g.90791346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791346G>T , CM000667.2:g.90791346G>T	GRCh38
NC_000005.9:g.90087163G>T , CM000667.1:g.90087163G>T	GRCh37
NC_000005.8:g.90122919G>T	NCBI36
NG_007083.1:g.237547G>T
NG_007083.2:g.267003G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14517G>T MANE Select	ENSP00000384582.2:p.Gln4839His
ENST00000425867.3:c.3471G>T	ENSP00000392618.3:p.Gln1157His
ENST00000507314.2:c.192G>T	ENSP00000491299.1:p.Gln64His
ENST00000638510.1:n.1784G>T
ENST00000638585.1:n.283G>T
ENST00000638975.1:c.1146G>T	ENSP00000492630.1:p.Gln382His
ENST00000639431.1:c.265+115137G>T	ENSP00000491057.1:n.265+115137G>T
ENST00000640407.1:c.927G>T	ENSP00000491425.1:p.Gln309His
ENST00000405460.6:c.14517G>T	ENSP00000384582.2:p.Gln4839His
ENST00000425867.2:c.1500G>T	ENSP00000392618.2:p.Gln500His
ENST00000507314.1:n.192G>T
NM_032119.3:c.14517G>T	NP_115495.3:p.Gln4839His
NR_003149.1:n.14530G>T
XM_011543675.1:c.14514G>T	XP_011541977.1:p.Gln4838His
XM_011543676.1:c.14436G>T	XP_011541978.1:p.Gln4812His
XM_011543677.1:c.11820G>T	XP_011541979.1:p.Gln3940His
XM_011543678.1:c.14517G>T	XP_011541980.1:p.Gln4839His
NM_032119.4:c.14517G>T MANE Select	NP_115495.3:p.Gln4839His
XM_017009963.2:c.14538G>T	XP_016865452.1:p.Gln4846His
XM_017009964.2:c.14535G>T	XP_016865453.1:p.Gln4845His
XM_017009965.1:c.14535G>T	XP_016865454.1:p.Gln4845His
XM_017009966.2:c.14457G>T	XP_016865455.1:p.Gln4819His
XM_017009967.1:c.14442G>T	XP_016865456.1:p.Gln4814His
XM_017009968.2:c.14538G>T	XP_016865457.1:p.Gln4846His
XM_017009969.2:c.14538G>T	XP_016865458.1:p.Gln4846His
XM_017009970.2:c.14538G>T	XP_016865459.1:p.Gln4846His
XM_017009971.2:c.14538G>T	XP_016865460.1:p.Gln4846His
XM_017009972.1:c.7656G>T	XP_016865461.1:p.Gln2552His
XM_017009973.1:c.7635G>T	XP_016865462.1:p.Gln2545His
NR_003149.2:n.14533G>T