Canonical Allele Identifier: CA360396236

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008159A>C (hg19) ; chr5:g.90712342A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712342A>C , CM000667.2:g.90712342A>C	GRCh38
NC_000005.9:g.90008159A>C , CM000667.1:g.90008159A>C	GRCh37
NC_000005.8:g.90043915A>C	NCBI36
NG_007083.1:g.158543A>C
NG_007083.2:g.187999A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9098A>C MANE Select	ENSP00000384582.2:p.Asp3033Ala
ENST00000639431.1:c.265+36133A>C	ENSP00000491057.1:n.265+36133A>C
ENST00000639473.1:n.4557A>C
ENST00000640012.1:c.2905A>C
ENST00000640374.1:n.2242A>C
ENST00000640779.1:c.3827A>C
ENST00000405460.6:c.9098A>C	ENSP00000384582.2:p.Asp3033Ala
ENST00000509621.1:c.1795A>C
NM_032119.3:c.9098A>C	NP_115495.3:p.Asp3033Ala
NR_003149.1:n.9111A>C
XM_011543675.1:c.9095A>C	XP_011541977.1:p.Asp3032Ala
XM_011543676.1:c.9017A>C	XP_011541978.1:p.Asp3006Ala
XM_011543677.1:c.6401A>C	XP_011541979.1:p.Asp2134Ala
XM_011543678.1:c.9098A>C	XP_011541980.1:p.Asp3033Ala
XM_011543679.1:c.9098A>C	XP_011541981.1:p.Asp3033Ala
NM_032119.4:c.9098A>C MANE Select	NP_115495.3:p.Asp3033Ala
XM_017009963.2:c.9119A>C	XP_016865452.1:p.Asp3040Ala
XM_017009964.2:c.9116A>C	XP_016865453.1:p.Asp3039Ala
XM_017009965.1:c.9116A>C	XP_016865454.1:p.Asp3039Ala
XM_017009966.2:c.9038A>C	XP_016865455.1:p.Asp3013Ala
XM_017009967.1:c.9023A>C	XP_016865456.1:p.Asp3008Ala
XM_017009968.2:c.9119A>C	XP_016865457.1:p.Asp3040Ala
XM_017009969.2:c.9119A>C	XP_016865458.1:p.Asp3040Ala
XM_017009970.2:c.9119A>C	XP_016865459.1:p.Asp3040Ala
XM_017009971.2:c.9119A>C	XP_016865460.1:p.Asp3040Ala
XM_017009972.1:c.2237A>C	XP_016865461.1:p.Asp746Ala
XM_017009973.1:c.2216A>C	XP_016865462.1:p.Asp739Ala
XM_017009974.2:c.9119A>C	XP_016865463.1:p.Asp3040Ala
NR_003149.2:n.9114A>C