Canonical Allele Identifier: CA360401293

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086927C>T (hg19) ; chr5:g.90791110C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791110C>T , CM000667.2:g.90791110C>T	GRCh38
NC_000005.9:g.90086927C>T , CM000667.1:g.90086927C>T	GRCh37
NC_000005.8:g.90122683C>T	NCBI36
NG_007083.1:g.237311C>T
NG_007083.2:g.266767C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14281C>T MANE Select	ENSP00000384582.2:p.His4761Tyr
ENST00000425867.3:c.3235C>T	ENSP00000392618.3:p.His1079Tyr
ENST00000638510.1:n.1548C>T
ENST00000638585.1:n.47C>T
ENST00000638975.1:c.910C>T	ENSP00000492630.1:p.His304Tyr
ENST00000639431.1:c.265+114901C>T	ENSP00000491057.1:n.265+114901C>T
ENST00000640407.1:c.691C>T	ENSP00000491425.1:p.His231Tyr
ENST00000405460.6:c.14281C>T	ENSP00000384582.2:p.His4761Tyr
ENST00000425867.2:c.1264C>T	ENSP00000392618.2:p.His422Tyr
NM_032119.3:c.14281C>T	NP_115495.3:p.His4761Tyr
NR_003149.1:n.14294C>T
XM_011543675.1:c.14278C>T	XP_011541977.1:p.His4760Tyr
XM_011543676.1:c.14200C>T	XP_011541978.1:p.His4734Tyr
XM_011543677.1:c.11584C>T	XP_011541979.1:p.His3862Tyr
XM_011543678.1:c.14281C>T	XP_011541980.1:p.His4761Tyr
NM_032119.4:c.14281C>T MANE Select	NP_115495.3:p.His4761Tyr
XM_017009963.2:c.14302C>T	XP_016865452.1:p.His4768Tyr
XM_017009964.2:c.14299C>T	XP_016865453.1:p.His4767Tyr
XM_017009965.1:c.14299C>T	XP_016865454.1:p.His4767Tyr
XM_017009966.2:c.14221C>T	XP_016865455.1:p.His4741Tyr
XM_017009967.1:c.14206C>T	XP_016865456.1:p.His4736Tyr
XM_017009968.2:c.14302C>T	XP_016865457.1:p.His4768Tyr
XM_017009969.2:c.14302C>T	XP_016865458.1:p.His4768Tyr
XM_017009970.2:c.14302C>T	XP_016865459.1:p.His4768Tyr
XM_017009971.2:c.14302C>T	XP_016865460.1:p.His4768Tyr
XM_017009972.1:c.7420C>T	XP_016865461.1:p.His2474Tyr
XM_017009973.1:c.7399C>T	XP_016865462.1:p.His2467Tyr
NR_003149.2:n.14297C>T