Canonical Allele Identifier: CA360366537

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050863T>G (hg19) ; chr5:g.90755046T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755046T>G , CM000667.2:g.90755046T>G	GRCh38
NC_000005.9:g.90050863T>G , CM000667.1:g.90050863T>G	GRCh37
NC_000005.8:g.90086619T>G	NCBI36
NG_007083.1:g.201247T>G
NG_007083.2:g.230703T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11441T>G MANE Select	ENSP00000384582.2:p.Ile3814Ser
ENST00000425867.3:c.572T>G	ENSP00000392618.3:p.Ile191Ser
ENST00000639431.1:c.265+78837T>G	ENSP00000491057.1:n.265+78837T>G
ENST00000640374.1:n.4585T>G
ENST00000640464.1:n.1860T>G
ENST00000405460.6:c.11441T>G	ENSP00000384582.2:p.Ile3814Ser
ENST00000509621.1:c.4138T>G
NM_032119.3:c.11441T>G	NP_115495.3:p.Ile3814Ser
NR_003149.1:n.11454T>G
XM_011543675.1:c.11438T>G	XP_011541977.1:p.Ile3813Ser
XM_011543676.1:c.11360T>G	XP_011541978.1:p.Ile3787Ser
XM_011543677.1:c.8744T>G	XP_011541979.1:p.Ile2915Ser
XM_011543678.1:c.11441T>G	XP_011541980.1:p.Ile3814Ser
NM_032119.4:c.11441T>G MANE Select	NP_115495.3:p.Ile3814Ser
XM_017009963.2:c.11462T>G	XP_016865452.1:p.Ile3821Ser
XM_017009964.2:c.11459T>G	XP_016865453.1:p.Ile3820Ser
XM_017009965.1:c.11459T>G	XP_016865454.1:p.Ile3820Ser
XM_017009966.2:c.11381T>G	XP_016865455.1:p.Ile3794Ser
XM_017009967.1:c.11366T>G	XP_016865456.1:p.Ile3789Ser
XM_017009968.2:c.11462T>G	XP_016865457.1:p.Ile3821Ser
XM_017009969.2:c.11462T>G	XP_016865458.1:p.Ile3821Ser
XM_017009970.2:c.11462T>G	XP_016865459.1:p.Ile3821Ser
XM_017009971.2:c.11462T>G	XP_016865460.1:p.Ile3821Ser
XM_017009972.1:c.4580T>G	XP_016865461.1:p.Ile1527Ser
XM_017009973.1:c.4559T>G	XP_016865462.1:p.Ile1520Ser
NR_003149.2:n.11457T>G