Canonical Allele Identifier: CA360409169

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041502A>C (hg19) ; chr5:g.90745685A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745685A>C , CM000667.2:g.90745685A>C	GRCh38
NC_000005.9:g.90041502A>C , CM000667.1:g.90041502A>C	GRCh37
NC_000005.8:g.90077258A>C	NCBI36
NG_007083.1:g.191886A>C
NG_007083.2:g.221342A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10864A>C MANE Select	ENSP00000384582.2:p.Lys3622Gln
ENST00000639431.1:c.265+69476A>C	ENSP00000491057.1:n.265+69476A>C
ENST00000640374.1:n.4008A>C
ENST00000640464.1:n.1283A>C
ENST00000405460.6:c.10864A>C	ENSP00000384582.2:p.Lys3622Gln
ENST00000509621.1:c.3561A>C
NM_032119.3:c.10864A>C	NP_115495.3:p.Lys3622Gln
NR_003149.1:n.10877A>C
XM_011543675.1:c.10861A>C	XP_011541977.1:p.Lys3621Gln
XM_011543676.1:c.10783A>C	XP_011541978.1:p.Lys3595Gln
XM_011543677.1:c.8167A>C	XP_011541979.1:p.Lys2723Gln
XM_011543678.1:c.10864A>C	XP_011541980.1:p.Lys3622Gln
XM_011543679.1:c.*86A>C	XP_011541981.1:n.*86A>C
NM_032119.4:c.10864A>C MANE Select	NP_115495.3:p.Lys3622Gln
XM_017009963.2:c.10885A>C	XP_016865452.1:p.Lys3629Gln
XM_017009964.2:c.10882A>C	XP_016865453.1:p.Lys3628Gln
XM_017009965.1:c.10882A>C	XP_016865454.1:p.Lys3628Gln
XM_017009966.2:c.10804A>C	XP_016865455.1:p.Lys3602Gln
XM_017009967.1:c.10789A>C	XP_016865456.1:p.Lys3597Gln
XM_017009968.2:c.10885A>C	XP_016865457.1:p.Lys3629Gln
XM_017009969.2:c.10885A>C	XP_016865458.1:p.Lys3629Gln
XM_017009970.2:c.10885A>C	XP_016865459.1:p.Lys3629Gln
XM_017009971.2:c.10885A>C	XP_016865460.1:p.Lys3629Gln
XM_017009972.1:c.4003A>C	XP_016865461.1:p.Lys1335Gln
XM_017009973.1:c.3982A>C	XP_016865462.1:p.Lys1328Gln
XM_017009974.2:c.*86A>C	XP_016865463.1:n.*86A>C
NR_003149.2:n.10880A>C