Canonical Allele Identifier: CA360396331

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008200T>G (hg19) ; chr5:g.90712383T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712383T>G , CM000667.2:g.90712383T>G	GRCh38
NC_000005.9:g.90008200T>G , CM000667.1:g.90008200T>G	GRCh37
NC_000005.8:g.90043956T>G	NCBI36
NG_007083.1:g.158584T>G
NG_007083.2:g.188040T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9139T>G MANE Select	ENSP00000384582.2:p.Leu3047Val
ENST00000639431.1:c.265+36174T>G	ENSP00000491057.1:n.265+36174T>G
ENST00000639473.1:n.4598T>G
ENST00000640012.1:c.2946T>G
ENST00000640374.1:n.2283T>G
ENST00000640779.1:c.3868T>G
ENST00000405460.6:c.9139T>G	ENSP00000384582.2:p.Leu3047Val
ENST00000509621.1:c.1836T>G
NM_032119.3:c.9139T>G	NP_115495.3:p.Leu3047Val
NR_003149.1:n.9152T>G
XM_011543675.1:c.9136T>G	XP_011541977.1:p.Leu3046Val
XM_011543676.1:c.9058T>G	XP_011541978.1:p.Leu3020Val
XM_011543677.1:c.6442T>G	XP_011541979.1:p.Leu2148Val
XM_011543678.1:c.9139T>G	XP_011541980.1:p.Leu3047Val
XM_011543679.1:c.9139T>G	XP_011541981.1:p.Leu3047Val
XR_948560.1:n.463A>C
NM_032119.4:c.9139T>G MANE Select	NP_115495.3:p.Leu3047Val
XM_017009963.2:c.9160T>G	XP_016865452.1:p.Leu3054Val
XM_017009964.2:c.9157T>G	XP_016865453.1:p.Leu3053Val
XM_017009965.1:c.9157T>G	XP_016865454.1:p.Leu3053Val
XM_017009966.2:c.9079T>G	XP_016865455.1:p.Leu3027Val
XM_017009967.1:c.9064T>G	XP_016865456.1:p.Leu3022Val
XM_017009968.2:c.9160T>G	XP_016865457.1:p.Leu3054Val
XM_017009969.2:c.9160T>G	XP_016865458.1:p.Leu3054Val
XM_017009970.2:c.9160T>G	XP_016865459.1:p.Leu3054Val
XM_017009971.2:c.9160T>G	XP_016865460.1:p.Leu3054Val
XM_017009972.1:c.2278T>G	XP_016865461.1:p.Leu760Val
XM_017009973.1:c.2257T>G	XP_016865462.1:p.Leu753Val
XM_017009974.2:c.9160T>G	XP_016865463.1:p.Leu3054Val
NR_003149.2:n.9155T>G