Canonical Allele Identifier: CA360388702

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89999497T>A (hg19) ; chr5:g.90703680T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703680T>A , CM000667.2:g.90703680T>A	GRCh38
NC_000005.9:g.89999497T>A , CM000667.1:g.89999497T>A	GRCh37
NC_000005.8:g.90035253T>A	NCBI36
NG_007083.1:g.149881T>A
NG_007083.2:g.179337T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8171T>A MANE Select	ENSP00000384582.2:p.Phe2724Tyr
ENST00000639431.1:c.265+27471T>A	ENSP00000491057.1:n.265+27471T>A
ENST00000639473.1:n.3630T>A
ENST00000640012.1:c.1978T>A
ENST00000640374.1:n.1315T>A
ENST00000640403.1:c.5462T>A	ENSP00000492531.1:p.Phe1821Tyr
ENST00000640779.1:c.2900T>A
ENST00000405460.6:c.8171T>A	ENSP00000384582.2:p.Phe2724Tyr
ENST00000509621.1:c.868T>A
NM_032119.3:c.8171T>A	NP_115495.3:p.Phe2724Tyr
NR_003149.1:n.8184T>A
XM_011543675.1:c.8168T>A	XP_011541977.1:p.Phe2723Tyr
XM_011543676.1:c.8090T>A	XP_011541978.1:p.Phe2697Tyr
XM_011543677.1:c.5474T>A	XP_011541979.1:p.Phe1825Tyr
XM_011543678.1:c.8171T>A	XP_011541980.1:p.Phe2724Tyr
XM_011543679.1:c.8171T>A	XP_011541981.1:p.Phe2724Tyr
NM_032119.4:c.8171T>A MANE Select	NP_115495.3:p.Phe2724Tyr
XM_017009963.2:c.8171T>A	XP_016865452.1:p.Phe2724Tyr
XM_017009964.2:c.8168T>A	XP_016865453.1:p.Phe2723Tyr
XM_017009965.1:c.8168T>A	XP_016865454.1:p.Phe2723Tyr
XM_017009966.2:c.8090T>A	XP_016865455.1:p.Phe2697Tyr
XM_017009967.1:c.8075T>A	XP_016865456.1:p.Phe2692Tyr
XM_017009968.2:c.8171T>A	XP_016865457.1:p.Phe2724Tyr
XM_017009969.2:c.8171T>A	XP_016865458.1:p.Phe2724Tyr
XM_017009970.2:c.8171T>A	XP_016865459.1:p.Phe2724Tyr
XM_017009971.2:c.8171T>A	XP_016865460.1:p.Phe2724Tyr
XM_017009972.1:c.1289T>A	XP_016865461.1:p.Phe430Tyr
XM_017009973.1:c.1289T>A	XP_016865462.1:p.Phe430Tyr
XM_017009974.2:c.8171T>A	XP_016865463.1:p.Phe2724Tyr
NR_003149.2:n.8187T>A