Canonical Allele Identifier: CA360366964

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050926A>C (hg19) ; chr5:g.90755109A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755109A>C , CM000667.2:g.90755109A>C	GRCh38
NC_000005.9:g.90050926A>C , CM000667.1:g.90050926A>C	GRCh37
NC_000005.8:g.90086682A>C	NCBI36
NG_007083.1:g.201310A>C
NG_007083.2:g.230766A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11504A>C MANE Select	ENSP00000384582.2:p.Asp3835Ala
ENST00000425867.3:c.635A>C	ENSP00000392618.3:p.Asp212Ala
ENST00000639431.1:c.265+78900A>C	ENSP00000491057.1:n.265+78900A>C
ENST00000640374.1:n.4648A>C
ENST00000640464.1:n.1923A>C
ENST00000405460.6:c.11504A>C	ENSP00000384582.2:p.Asp3835Ala
ENST00000509621.1:c.4201A>C
NM_032119.3:c.11504A>C	NP_115495.3:p.Asp3835Ala
NR_003149.1:n.11517A>C
XM_011543675.1:c.11501A>C	XP_011541977.1:p.Asp3834Ala
XM_011543676.1:c.11423A>C	XP_011541978.1:p.Asp3808Ala
XM_011543677.1:c.8807A>C	XP_011541979.1:p.Asp2936Ala
XM_011543678.1:c.11504A>C	XP_011541980.1:p.Asp3835Ala
NM_032119.4:c.11504A>C MANE Select	NP_115495.3:p.Asp3835Ala
XM_017009963.2:c.11525A>C	XP_016865452.1:p.Asp3842Ala
XM_017009964.2:c.11522A>C	XP_016865453.1:p.Asp3841Ala
XM_017009965.1:c.11522A>C	XP_016865454.1:p.Asp3841Ala
XM_017009966.2:c.11444A>C	XP_016865455.1:p.Asp3815Ala
XM_017009967.1:c.11429A>C	XP_016865456.1:p.Asp3810Ala
XM_017009968.2:c.11525A>C	XP_016865457.1:p.Asp3842Ala
XM_017009969.2:c.11525A>C	XP_016865458.1:p.Asp3842Ala
XM_017009970.2:c.11525A>C	XP_016865459.1:p.Asp3842Ala
XM_017009971.2:c.11525A>C	XP_016865460.1:p.Asp3842Ala
XM_017009972.1:c.4643A>C	XP_016865461.1:p.Asp1548Ala
XM_017009973.1:c.4622A>C	XP_016865462.1:p.Asp1541Ala
NR_003149.2:n.11520A>C