Canonical Allele Identifier: CA360367075

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050942A>C (hg19) ; chr5:g.90755125A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755125A>C , CM000667.2:g.90755125A>C	GRCh38
NC_000005.9:g.90050942A>C , CM000667.1:g.90050942A>C	GRCh37
NC_000005.8:g.90086698A>C	NCBI36
NG_007083.1:g.201326A>C
NG_007083.2:g.230782A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11520A>C MANE Select	ENSP00000384582.2:p.Glu3840Asp
ENST00000425867.3:c.651A>C	ENSP00000392618.3:p.Glu217Asp
ENST00000639431.1:c.265+78916A>C	ENSP00000491057.1:n.265+78916A>C
ENST00000640374.1:n.4664A>C
ENST00000640464.1:n.1939A>C
ENST00000405460.6:c.11520A>C	ENSP00000384582.2:p.Glu3840Asp
ENST00000509621.1:c.4217A>C
NM_032119.3:c.11520A>C	NP_115495.3:p.Glu3840Asp
NR_003149.1:n.11533A>C
XM_011543675.1:c.11517A>C	XP_011541977.1:p.Glu3839Asp
XM_011543676.1:c.11439A>C	XP_011541978.1:p.Glu3813Asp
XM_011543677.1:c.8823A>C	XP_011541979.1:p.Glu2941Asp
XM_011543678.1:c.11520A>C	XP_011541980.1:p.Glu3840Asp
NM_032119.4:c.11520A>C MANE Select	NP_115495.3:p.Glu3840Asp
XM_017009963.2:c.11541A>C	XP_016865452.1:p.Glu3847Asp
XM_017009964.2:c.11538A>C	XP_016865453.1:p.Glu3846Asp
XM_017009965.1:c.11538A>C	XP_016865454.1:p.Glu3846Asp
XM_017009966.2:c.11460A>C	XP_016865455.1:p.Glu3820Asp
XM_017009967.1:c.11445A>C	XP_016865456.1:p.Glu3815Asp
XM_017009968.2:c.11541A>C	XP_016865457.1:p.Glu3847Asp
XM_017009969.2:c.11541A>C	XP_016865458.1:p.Glu3847Asp
XM_017009970.2:c.11541A>C	XP_016865459.1:p.Glu3847Asp
XM_017009971.2:c.11541A>C	XP_016865460.1:p.Glu3847Asp
XM_017009972.1:c.4659A>C	XP_016865461.1:p.Glu1553Asp
XM_017009973.1:c.4638A>C	XP_016865462.1:p.Glu1546Asp
NR_003149.2:n.11536A>C