Canonical Allele Identifier: CA360401702

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087026T>A (hg19) ; chr5:g.90791209T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791209T>A , CM000667.2:g.90791209T>A	GRCh38
NC_000005.9:g.90087026T>A , CM000667.1:g.90087026T>A	GRCh37
NC_000005.8:g.90122782T>A	NCBI36
NG_007083.1:g.237410T>A
NG_007083.2:g.266866T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14380T>A MANE Select	ENSP00000384582.2:p.Phe4794Ile
ENST00000425867.3:c.3334T>A	ENSP00000392618.3:p.Phe1112Ile
ENST00000507314.2:c.55T>A	ENSP00000491299.1:p.Phe19Ile
ENST00000638510.1:n.1647T>A
ENST00000638585.1:n.146T>A
ENST00000638975.1:c.1009T>A	ENSP00000492630.1:p.Phe337Ile
ENST00000639431.1:c.265+115000T>A	ENSP00000491057.1:n.265+115000T>A
ENST00000640407.1:c.790T>A	ENSP00000491425.1:p.Phe264Ile
ENST00000405460.6:c.14380T>A	ENSP00000384582.2:p.Phe4794Ile
ENST00000425867.2:c.1363T>A	ENSP00000392618.2:p.Phe455Ile
ENST00000507314.1:n.55T>A
NM_032119.3:c.14380T>A	NP_115495.3:p.Phe4794Ile
NR_003149.1:n.14393T>A
XM_011543675.1:c.14377T>A	XP_011541977.1:p.Phe4793Ile
XM_011543676.1:c.14299T>A	XP_011541978.1:p.Phe4767Ile
XM_011543677.1:c.11683T>A	XP_011541979.1:p.Phe3895Ile
XM_011543678.1:c.14380T>A	XP_011541980.1:p.Phe4794Ile
NM_032119.4:c.14380T>A MANE Select	NP_115495.3:p.Phe4794Ile
XM_017009963.2:c.14401T>A	XP_016865452.1:p.Phe4801Ile
XM_017009964.2:c.14398T>A	XP_016865453.1:p.Phe4800Ile
XM_017009965.1:c.14398T>A	XP_016865454.1:p.Phe4800Ile
XM_017009966.2:c.14320T>A	XP_016865455.1:p.Phe4774Ile
XM_017009967.1:c.14305T>A	XP_016865456.1:p.Phe4769Ile
XM_017009968.2:c.14401T>A	XP_016865457.1:p.Phe4801Ile
XM_017009969.2:c.14401T>A	XP_016865458.1:p.Phe4801Ile
XM_017009970.2:c.14401T>A	XP_016865459.1:p.Phe4801Ile
XM_017009971.2:c.14401T>A	XP_016865460.1:p.Phe4801Ile
XM_017009972.1:c.7519T>A	XP_016865461.1:p.Phe2507Ile
XM_017009973.1:c.7498T>A	XP_016865462.1:p.Phe2500Ile
NR_003149.2:n.14396T>A