Canonical Allele Identifier: CA360409716

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106559T>G (hg19) ; chr5:g.90810742T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810742T>G , CM000667.2:g.90810742T>G	GRCh38
NC_000005.9:g.90106559T>G , CM000667.1:g.90106559T>G	GRCh37
NC_000005.8:g.90142315T>G	NCBI36
NG_007083.1:g.256943T>G
NG_007083.2:g.286399T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15482T>G MANE Select	ENSP00000384582.2:p.Leu5161Arg
ENST00000425867.3:c.4436T>G	ENSP00000392618.3:p.Leu1479Arg
ENST00000638510.1:n.2749T>G
ENST00000639431.1:c.265+134533T>G	ENSP00000491057.1:n.265+134533T>G
ENST00000640407.1:c.1892T>G	ENSP00000491425.1:p.Leu631Arg
ENST00000405460.6:c.15482T>G	ENSP00000384582.2:p.Leu5161Arg
ENST00000425867.2:c.2465T>G	ENSP00000392618.2:p.Leu822Arg
NM_032119.3:c.15482T>G	NP_115495.3:p.Leu5161Arg
NR_003149.1:n.15495T>G
XM_011543675.1:c.15479T>G	XP_011541977.1:p.Leu5160Arg
XM_011543676.1:c.15401T>G	XP_011541978.1:p.Leu5134Arg
XM_011543677.1:c.12785T>G	XP_011541979.1:p.Leu4262Arg
NM_032119.4:c.15482T>G MANE Select	NP_115495.3:p.Leu5161Arg
XM_017009963.2:c.15503T>G	XP_016865452.1:p.Leu5168Arg
XM_017009964.2:c.15500T>G	XP_016865453.1:p.Leu5167Arg
XM_017009965.1:c.15500T>G	XP_016865454.1:p.Leu5167Arg
XM_017009966.2:c.15422T>G	XP_016865455.1:p.Leu5141Arg
XM_017009967.1:c.15407T>G	XP_016865456.1:p.Leu5136Arg
XM_017009968.2:c.15323T>G	XP_016865457.1:p.Leu5108Arg
XM_017009969.2:c.15503T>G	XP_016865458.1:p.Leu5168Arg
XM_017009971.2:c.*436T>G	XP_016865460.1:n.*436T>G
XM_017009972.1:c.8621T>G	XP_016865461.1:p.Leu2874Arg
XM_017009973.1:c.8600T>G	XP_016865462.1:p.Leu2867Arg
NR_003149.2:n.15498T>G