Canonical Allele Identifier: CA360414473

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979998T>C (hg19) ; chr5:g.90684181T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684181T>C , CM000667.2:g.90684181T>C	GRCh38
NC_000005.9:g.89979998T>C , CM000667.1:g.89979998T>C	GRCh37
NC_000005.8:g.90015754T>C	NCBI36
NG_007083.1:g.130382T>C
NG_007083.2:g.159838T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6260T>C MANE Select	ENSP00000384582.2:p.Val2087Ala
ENST00000639431.1:c.265+7972T>C	ENSP00000491057.1:n.265+7972T>C
ENST00000639473.1:n.1719T>C
ENST00000640012.1:c.165-1599T>C
ENST00000640403.1:c.3551T>C	ENSP00000492531.1:p.Val1184Ala
ENST00000640779.1:c.1072T>C
ENST00000405460.6:c.6260T>C	ENSP00000384582.2:p.Val2087Ala
NM_032119.3:c.6260T>C	NP_115495.3:p.Val2087Ala
NR_003149.1:n.6356T>C
XM_011543675.1:c.6257T>C	XP_011541977.1:p.Val2086Ala
XM_011543676.1:c.6179T>C	XP_011541978.1:p.Val2060Ala
XM_011543677.1:c.3563T>C	XP_011541979.1:p.Val1188Ala
XM_011543678.1:c.6260T>C	XP_011541980.1:p.Val2087Ala
XM_011543679.1:c.6260T>C	XP_011541981.1:p.Val2087Ala
NM_032119.4:c.6260T>C MANE Select	NP_115495.3:p.Val2087Ala
XM_017009963.2:c.6260T>C	XP_016865452.1:p.Val2087Ala
XM_017009964.2:c.6257T>C	XP_016865453.1:p.Val2086Ala
XM_017009965.1:c.6257T>C	XP_016865454.1:p.Val2086Ala
XM_017009966.2:c.6179T>C	XP_016865455.1:p.Val2060Ala
XM_017009967.1:c.6164T>C	XP_016865456.1:p.Val2055Ala
XM_017009968.2:c.6260T>C	XP_016865457.1:p.Val2087Ala
XM_017009969.2:c.6260T>C	XP_016865458.1:p.Val2087Ala
XM_017009970.2:c.6260T>C	XP_016865459.1:p.Val2087Ala
XM_017009971.2:c.6260T>C	XP_016865460.1:p.Val2087Ala
XM_017009973.1:c.-540T>C	XP_016865462.1:n.-540T>C
XM_017009974.2:c.6260T>C	XP_016865463.1:p.Val2087Ala
NR_003149.2:n.6359T>C