Canonical Allele Identifier: CA360401707

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1274500653
• MyVariant Identifiers: chr5:g.90087027T>A (hg19) ; chr5:g.90791210T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791210T>A , CM000667.2:g.90791210T>A	GRCh38
NC_000005.9:g.90087027T>A , CM000667.1:g.90087027T>A	GRCh37
NC_000005.8:g.90122783T>A	NCBI36
NG_007083.1:g.237411T>A
NG_007083.2:g.266867T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14381T>A MANE Select	ENSP00000384582.2:p.Phe4794Tyr
ENST00000425867.3:c.3335T>A	ENSP00000392618.3:p.Phe1112Tyr
ENST00000507314.2:c.56T>A	ENSP00000491299.1:p.Phe19Tyr
ENST00000638510.1:n.1648T>A
ENST00000638585.1:n.147T>A
ENST00000638975.1:c.1010T>A	ENSP00000492630.1:p.Phe337Tyr
ENST00000639431.1:c.265+115001T>A	ENSP00000491057.1:n.265+115001T>A
ENST00000640407.1:c.791T>A	ENSP00000491425.1:p.Phe264Tyr
ENST00000405460.6:c.14381T>A	ENSP00000384582.2:p.Phe4794Tyr
ENST00000425867.2:c.1364T>A	ENSP00000392618.2:p.Phe455Tyr
ENST00000507314.1:n.56T>A
NM_032119.3:c.14381T>A	NP_115495.3:p.Phe4794Tyr
NR_003149.1:n.14394T>A
XM_011543675.1:c.14378T>A	XP_011541977.1:p.Phe4793Tyr
XM_011543676.1:c.14300T>A	XP_011541978.1:p.Phe4767Tyr
XM_011543677.1:c.11684T>A	XP_011541979.1:p.Phe3895Tyr
XM_011543678.1:c.14381T>A	XP_011541980.1:p.Phe4794Tyr
NM_032119.4:c.14381T>A MANE Select	NP_115495.3:p.Phe4794Tyr
XM_017009963.2:c.14402T>A	XP_016865452.1:p.Phe4801Tyr
XM_017009964.2:c.14399T>A	XP_016865453.1:p.Phe4800Tyr
XM_017009965.1:c.14399T>A	XP_016865454.1:p.Phe4800Tyr
XM_017009966.2:c.14321T>A	XP_016865455.1:p.Phe4774Tyr
XM_017009967.1:c.14306T>A	XP_016865456.1:p.Phe4769Tyr
XM_017009968.2:c.14402T>A	XP_016865457.1:p.Phe4801Tyr
XM_017009969.2:c.14402T>A	XP_016865458.1:p.Phe4801Tyr
XM_017009970.2:c.14402T>A	XP_016865459.1:p.Phe4801Tyr
XM_017009971.2:c.14402T>A	XP_016865460.1:p.Phe4801Tyr
XM_017009972.1:c.7520T>A	XP_016865461.1:p.Phe2507Tyr
XM_017009973.1:c.7499T>A	XP_016865462.1:p.Phe2500Tyr
NR_003149.2:n.14397T>A