Canonical Allele Identifier: CA360396147

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008120A>C (hg19) ; chr5:g.90712303A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712303A>C , CM000667.2:g.90712303A>C	GRCh38
NC_000005.9:g.90008120A>C , CM000667.1:g.90008120A>C	GRCh37
NC_000005.8:g.90043876A>C	NCBI36
NG_007083.1:g.158504A>C
NG_007083.2:g.187960A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9059A>C MANE Select	ENSP00000384582.2:p.Asp3020Ala
ENST00000639431.1:c.265+36094A>C	ENSP00000491057.1:n.265+36094A>C
ENST00000639473.1:n.4518A>C
ENST00000640012.1:c.2866A>C
ENST00000640374.1:n.2203A>C
ENST00000640779.1:c.3788A>C
ENST00000405460.6:c.9059A>C	ENSP00000384582.2:p.Asp3020Ala
ENST00000509621.1:c.1756A>C
NM_032119.3:c.9059A>C	NP_115495.3:p.Asp3020Ala
NR_003149.1:n.9072A>C
XM_011543675.1:c.9056A>C	XP_011541977.1:p.Asp3019Ala
XM_011543676.1:c.8978A>C	XP_011541978.1:p.Asp2993Ala
XM_011543677.1:c.6362A>C	XP_011541979.1:p.Asp2121Ala
XM_011543678.1:c.9059A>C	XP_011541980.1:p.Asp3020Ala
XM_011543679.1:c.9059A>C	XP_011541981.1:p.Asp3020Ala
NM_032119.4:c.9059A>C MANE Select	NP_115495.3:p.Asp3020Ala
XM_017009963.2:c.9080A>C	XP_016865452.1:p.Asp3027Ala
XM_017009964.2:c.9077A>C	XP_016865453.1:p.Asp3026Ala
XM_017009965.1:c.9077A>C	XP_016865454.1:p.Asp3026Ala
XM_017009966.2:c.8999A>C	XP_016865455.1:p.Asp3000Ala
XM_017009967.1:c.8984A>C	XP_016865456.1:p.Asp2995Ala
XM_017009968.2:c.9080A>C	XP_016865457.1:p.Asp3027Ala
XM_017009969.2:c.9080A>C	XP_016865458.1:p.Asp3027Ala
XM_017009970.2:c.9080A>C	XP_016865459.1:p.Asp3027Ala
XM_017009971.2:c.9080A>C	XP_016865460.1:p.Asp3027Ala
XM_017009972.1:c.2198A>C	XP_016865461.1:p.Asp733Ala
XM_017009973.1:c.2177A>C	XP_016865462.1:p.Asp726Ala
XM_017009974.2:c.9080A>C	XP_016865463.1:p.Asp3027Ala
NR_003149.2:n.9075A>C