Canonical Allele Identifier: CA360397770

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012527A>C (hg19) ; chr5:g.90716710A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716710A>C , CM000667.2:g.90716710A>C	GRCh38
NC_000005.9:g.90012527A>C , CM000667.1:g.90012527A>C	GRCh37
NC_000005.8:g.90048283A>C	NCBI36
NG_007083.1:g.162911A>C
NG_007083.2:g.192367A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9428A>C MANE Select	ENSP00000384582.2:p.Glu3143Ala
ENST00000639431.1:c.265+40501A>C	ENSP00000491057.1:n.265+40501A>C
ENST00000639473.1:n.4887A>C
ENST00000640012.1:c.3235A>C
ENST00000640374.1:n.2572A>C
ENST00000640779.1:c.4157A>C
ENST00000405460.6:c.9428A>C	ENSP00000384582.2:p.Glu3143Ala
ENST00000509621.1:c.2125A>C
NM_032119.3:c.9428A>C	NP_115495.3:p.Glu3143Ala
NR_003149.1:n.9441A>C
XM_011543675.1:c.9425A>C	XP_011541977.1:p.Glu3142Ala
XM_011543676.1:c.9347A>C	XP_011541978.1:p.Glu3116Ala
XM_011543677.1:c.6731A>C	XP_011541979.1:p.Glu2244Ala
XM_011543678.1:c.9428A>C	XP_011541980.1:p.Glu3143Ala
XM_011543679.1:c.9428A>C	XP_011541981.1:p.Glu3143Ala
XR_948560.1:n.272-901T>G
NM_032119.4:c.9428A>C MANE Select	NP_115495.3:p.Glu3143Ala
XM_017009963.2:c.9449A>C	XP_016865452.1:p.Glu3150Ala
XM_017009964.2:c.9446A>C	XP_016865453.1:p.Glu3149Ala
XM_017009965.1:c.9446A>C	XP_016865454.1:p.Glu3149Ala
XM_017009966.2:c.9368A>C	XP_016865455.1:p.Glu3123Ala
XM_017009967.1:c.9353A>C	XP_016865456.1:p.Glu3118Ala
XM_017009968.2:c.9449A>C	XP_016865457.1:p.Glu3150Ala
XM_017009969.2:c.9449A>C	XP_016865458.1:p.Glu3150Ala
XM_017009970.2:c.9449A>C	XP_016865459.1:p.Glu3150Ala
XM_017009971.2:c.9449A>C	XP_016865460.1:p.Glu3150Ala
XM_017009972.1:c.2567A>C	XP_016865461.1:p.Glu856Ala
XM_017009973.1:c.2546A>C	XP_016865462.1:p.Glu849Ala
XM_017009974.2:c.9449A>C	XP_016865463.1:p.Glu3150Ala
XR_001742802.1:n.2523-901T>G
NR_003149.2:n.9444A>C