Canonical Allele Identifier: CA360366796

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050899T>C (hg19) ; chr5:g.90755082T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755082T>C , CM000667.2:g.90755082T>C	GRCh38
NC_000005.9:g.90050899T>C , CM000667.1:g.90050899T>C	GRCh37
NC_000005.8:g.90086655T>C	NCBI36
NG_007083.1:g.201283T>C
NG_007083.2:g.230739T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11477T>C MANE Select	ENSP00000384582.2:p.Val3826Ala
ENST00000425867.3:c.608T>C	ENSP00000392618.3:p.Val203Ala
ENST00000639431.1:c.265+78873T>C	ENSP00000491057.1:n.265+78873T>C
ENST00000640374.1:n.4621T>C
ENST00000640464.1:n.1896T>C
ENST00000405460.6:c.11477T>C	ENSP00000384582.2:p.Val3826Ala
ENST00000509621.1:c.4174T>C
NM_032119.3:c.11477T>C	NP_115495.3:p.Val3826Ala
NR_003149.1:n.11490T>C
XM_011543675.1:c.11474T>C	XP_011541977.1:p.Val3825Ala
XM_011543676.1:c.11396T>C	XP_011541978.1:p.Val3799Ala
XM_011543677.1:c.8780T>C	XP_011541979.1:p.Val2927Ala
XM_011543678.1:c.11477T>C	XP_011541980.1:p.Val3826Ala
NM_032119.4:c.11477T>C MANE Select	NP_115495.3:p.Val3826Ala
XM_017009963.2:c.11498T>C	XP_016865452.1:p.Val3833Ala
XM_017009964.2:c.11495T>C	XP_016865453.1:p.Val3832Ala
XM_017009965.1:c.11495T>C	XP_016865454.1:p.Val3832Ala
XM_017009966.2:c.11417T>C	XP_016865455.1:p.Val3806Ala
XM_017009967.1:c.11402T>C	XP_016865456.1:p.Val3801Ala
XM_017009968.2:c.11498T>C	XP_016865457.1:p.Val3833Ala
XM_017009969.2:c.11498T>C	XP_016865458.1:p.Val3833Ala
XM_017009970.2:c.11498T>C	XP_016865459.1:p.Val3833Ala
XM_017009971.2:c.11498T>C	XP_016865460.1:p.Val3833Ala
XM_017009972.1:c.4616T>C	XP_016865461.1:p.Val1539Ala
XM_017009973.1:c.4595T>C	XP_016865462.1:p.Val1532Ala
NR_003149.2:n.11493T>C