Canonical Allele Identifier: CA360401194

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086913C>A (hg19) ; chr5:g.90791096C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791096C>A , CM000667.2:g.90791096C>A	GRCh38
NC_000005.9:g.90086913C>A , CM000667.1:g.90086913C>A	GRCh37
NC_000005.8:g.90122669C>A	NCBI36
NG_007083.1:g.237297C>A
NG_007083.2:g.266753C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14267C>A MANE Select	ENSP00000384582.2:p.Ala4756Glu
ENST00000425867.3:c.3221C>A	ENSP00000392618.3:p.Ala1074Glu
ENST00000638510.1:n.1534C>A
ENST00000638585.1:n.33C>A
ENST00000638975.1:c.896C>A	ENSP00000492630.1:p.Ala299Glu
ENST00000639431.1:c.265+114887C>A	ENSP00000491057.1:n.265+114887C>A
ENST00000640407.1:c.677C>A	ENSP00000491425.1:p.Ala226Glu
ENST00000405460.6:c.14267C>A	ENSP00000384582.2:p.Ala4756Glu
ENST00000425867.2:c.1250C>A	ENSP00000392618.2:p.Ala417Glu
NM_032119.3:c.14267C>A	NP_115495.3:p.Ala4756Glu
NR_003149.1:n.14280C>A
XM_011543675.1:c.14264C>A	XP_011541977.1:p.Ala4755Glu
XM_011543676.1:c.14186C>A	XP_011541978.1:p.Ala4729Glu
XM_011543677.1:c.11570C>A	XP_011541979.1:p.Ala3857Glu
XM_011543678.1:c.14267C>A	XP_011541980.1:p.Ala4756Glu
NM_032119.4:c.14267C>A MANE Select	NP_115495.3:p.Ala4756Glu
XM_017009963.2:c.14288C>A	XP_016865452.1:p.Ala4763Glu
XM_017009964.2:c.14285C>A	XP_016865453.1:p.Ala4762Glu
XM_017009965.1:c.14285C>A	XP_016865454.1:p.Ala4762Glu
XM_017009966.2:c.14207C>A	XP_016865455.1:p.Ala4736Glu
XM_017009967.1:c.14192C>A	XP_016865456.1:p.Ala4731Glu
XM_017009968.2:c.14288C>A	XP_016865457.1:p.Ala4763Glu
XM_017009969.2:c.14288C>A	XP_016865458.1:p.Ala4763Glu
XM_017009970.2:c.14288C>A	XP_016865459.1:p.Ala4763Glu
XM_017009971.2:c.14288C>A	XP_016865460.1:p.Ala4763Glu
XM_017009972.1:c.7406C>A	XP_016865461.1:p.Ala2469Glu
XM_017009973.1:c.7385C>A	XP_016865462.1:p.Ala2462Glu
NR_003149.2:n.14283C>A