Canonical Allele Identifier: CA360401203

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14267C>T MANE Select	ENSP00000384582.2:p.Ala4756Val
ENST00000425867.3:c.3221C>T	ENSP00000392618.3:p.Ala1074Val
ENST00000638510.1:n.1534C>T
ENST00000638585.1:n.33C>T
ENST00000638975.1:c.896C>T	ENSP00000492630.1:p.Ala299Val
ENST00000639431.1:c.265+114887C>T	ENSP00000491057.1:n.265+114887C>T
ENST00000640407.1:c.677C>T	ENSP00000491425.1:p.Ala226Val
ENST00000405460.6:c.14267C>T	ENSP00000384582.2:p.Ala4756Val
ENST00000425867.2:c.1250C>T	ENSP00000392618.2:p.Ala417Val
NM_032119.3:c.14267C>T	NP_115495.3:p.Ala4756Val
NR_003149.1:n.14280C>T
XM_011543675.1:c.14264C>T	XP_011541977.1:p.Ala4755Val
XM_011543676.1:c.14186C>T	XP_011541978.1:p.Ala4729Val
XM_011543677.1:c.11570C>T	XP_011541979.1:p.Ala3857Val
XM_011543678.1:c.14267C>T	XP_011541980.1:p.Ala4756Val
NM_032119.4:c.14267C>T MANE Select	NP_115495.3:p.Ala4756Val
XM_017009963.2:c.14288C>T	XP_016865452.1:p.Ala4763Val
XM_017009964.2:c.14285C>T	XP_016865453.1:p.Ala4762Val
XM_017009965.1:c.14285C>T	XP_016865454.1:p.Ala4762Val
XM_017009966.2:c.14207C>T	XP_016865455.1:p.Ala4736Val
XM_017009967.1:c.14192C>T	XP_016865456.1:p.Ala4731Val
XM_017009968.2:c.14288C>T	XP_016865457.1:p.Ala4763Val
XM_017009969.2:c.14288C>T	XP_016865458.1:p.Ala4763Val
XM_017009970.2:c.14288C>T	XP_016865459.1:p.Ala4763Val
XM_017009971.2:c.14288C>T	XP_016865460.1:p.Ala4763Val
XM_017009972.1:c.7406C>T	XP_016865461.1:p.Ala2469Val
XM_017009973.1:c.7385C>T	XP_016865462.1:p.Ala2462Val
NR_003149.2:n.14283C>T