Canonical Allele Identifier: CA445467518

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086929T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791112T>C , CM000667.2:g.90791112T>C	GRCh38
NC_000005.9:g.90086929T>C , CM000667.1:g.90086929T>C	GRCh37
NC_000005.8:g.90122685T>C	NCBI36
NG_007083.1:g.237313T>C
NG_007083.2:g.266769T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14283T>C MANE Select	ENSP00000384582.2:p.His4761=
ENST00000425867.3:c.3237T>C	ENSP00000392618.3:p.His1079=
ENST00000638510.1:n.1550T>C
ENST00000638585.1:n.49T>C
ENST00000638975.1:c.912T>C	ENSP00000492630.1:p.His304=
ENST00000639431.1:c.265+114903T>C	ENSP00000491057.1:n.265+114903T>C
ENST00000640407.1:c.693T>C	ENSP00000491425.1:p.His231=
ENST00000405460.6:c.14283T>C	ENSP00000384582.2:p.His4761=
ENST00000425867.2:c.1266T>C	ENSP00000392618.2:p.His422=
NM_032119.3:c.14283T>C	NP_115495.3:p.His4761=
NR_003149.1:n.14296T>C
XM_011543675.1:c.14280T>C	XP_011541977.1:p.His4760=
XM_011543676.1:c.14202T>C	XP_011541978.1:p.His4734=
XM_011543677.1:c.11586T>C	XP_011541979.1:p.His3862=
XM_011543678.1:c.14283T>C	XP_011541980.1:p.His4761=
NM_032119.4:c.14283T>C MANE Select	NP_115495.3:p.His4761=
XM_017009963.2:c.14304T>C	XP_016865452.1:p.His4768=
XM_017009964.2:c.14301T>C	XP_016865453.1:p.His4767=
XM_017009965.1:c.14301T>C	XP_016865454.1:p.His4767=
XM_017009966.2:c.14223T>C	XP_016865455.1:p.His4741=
XM_017009967.1:c.14208T>C	XP_016865456.1:p.His4736=
XM_017009968.2:c.14304T>C	XP_016865457.1:p.His4768=
XM_017009969.2:c.14304T>C	XP_016865458.1:p.His4768=
XM_017009970.2:c.14304T>C	XP_016865459.1:p.His4768=
XM_017009971.2:c.14304T>C	XP_016865460.1:p.His4768=
XM_017009972.1:c.7422T>C	XP_016865461.1:p.His2474=
XM_017009973.1:c.7401T>C	XP_016865462.1:p.His2467=
NR_003149.2:n.14299T>C