Canonical Allele Identifier: CA360396237

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9098A>T MANE Select	ENSP00000384582.2:p.Asp3033Val
ENST00000639431.1:c.265+36133A>T	ENSP00000491057.1:n.265+36133A>T
ENST00000639473.1:n.4557A>T
ENST00000640012.1:c.2905A>T
ENST00000640374.1:n.2242A>T
ENST00000640779.1:c.3827A>T
ENST00000405460.6:c.9098A>T	ENSP00000384582.2:p.Asp3033Val
ENST00000509621.1:c.1795A>T
NM_032119.3:c.9098A>T	NP_115495.3:p.Asp3033Val
NR_003149.1:n.9111A>T
XM_011543675.1:c.9095A>T	XP_011541977.1:p.Asp3032Val
XM_011543676.1:c.9017A>T	XP_011541978.1:p.Asp3006Val
XM_011543677.1:c.6401A>T	XP_011541979.1:p.Asp2134Val
XM_011543678.1:c.9098A>T	XP_011541980.1:p.Asp3033Val
XM_011543679.1:c.9098A>T	XP_011541981.1:p.Asp3033Val
NM_032119.4:c.9098A>T MANE Select	NP_115495.3:p.Asp3033Val
XM_017009963.2:c.9119A>T	XP_016865452.1:p.Asp3040Val
XM_017009964.2:c.9116A>T	XP_016865453.1:p.Asp3039Val
XM_017009965.1:c.9116A>T	XP_016865454.1:p.Asp3039Val
XM_017009966.2:c.9038A>T	XP_016865455.1:p.Asp3013Val
XM_017009967.1:c.9023A>T	XP_016865456.1:p.Asp3008Val
XM_017009968.2:c.9119A>T	XP_016865457.1:p.Asp3040Val
XM_017009969.2:c.9119A>T	XP_016865458.1:p.Asp3040Val
XM_017009970.2:c.9119A>T	XP_016865459.1:p.Asp3040Val
XM_017009971.2:c.9119A>T	XP_016865460.1:p.Asp3040Val
XM_017009972.1:c.2237A>T	XP_016865461.1:p.Asp746Val
XM_017009973.1:c.2216A>T	XP_016865462.1:p.Asp739Val
XM_017009974.2:c.9119A>T	XP_016865463.1:p.Asp3040Val
NR_003149.2:n.9114A>T