Canonical Allele Identifier: CA360425653

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119349G>T (hg19) ; chr5:g.90823532G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823532G>T , CM000667.2:g.90823532G>T	GRCh38
NC_000005.9:g.90119349G>T , CM000667.1:g.90119349G>T	GRCh37
NC_000005.8:g.90155105G>T	NCBI36
NG_007083.1:g.269733G>T
NG_007083.2:g.299189G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16304G>T MANE Select	ENSP00000384582.2:p.Gly5435Val
ENST00000425867.3:c.5258G>T	ENSP00000392618.3:p.Gly1753Val
ENST00000638510.1:n.3571G>T
ENST00000639431.1:c.265+147323G>T	ENSP00000491057.1:n.265+147323G>T
ENST00000640061.1:n.128+1350G>T
ENST00000640407.1:c.2714G>T	ENSP00000491425.1:p.Gly905Val
ENST00000405460.6:c.16304G>T	ENSP00000384582.2:p.Gly5435Val
ENST00000425867.2:c.3287G>T	ENSP00000392618.2:p.Gly1096Val
NM_032119.3:c.16304G>T	NP_115495.3:p.Gly5435Val
NR_003149.1:n.16317G>T
XM_011543675.1:c.16301G>T	XP_011541977.1:p.Gly5434Val
XM_011543676.1:c.16223G>T	XP_011541978.1:p.Gly5408Val
XM_011543677.1:c.13607G>T	XP_011541979.1:p.Gly4536Val
NM_032119.4:c.16304G>T MANE Select	NP_115495.3:p.Gly5435Val
XM_017009963.2:c.16325G>T	XP_016865452.1:p.Gly5442Val
XM_017009964.2:c.16322G>T	XP_016865453.1:p.Gly5441Val
XM_017009965.1:c.16322G>T	XP_016865454.1:p.Gly5441Val
XM_017009966.2:c.16244G>T	XP_016865455.1:p.Gly5415Val
XM_017009967.1:c.16229G>T	XP_016865456.1:p.Gly5410Val
XM_017009968.2:c.16145G>T	XP_016865457.1:p.Gly5382Val
XM_017009969.2:c.16325G>T	XP_016865458.1:p.Gly5442Val
XM_017009972.1:c.9443G>T	XP_016865461.1:p.Gly3148Val
XM_017009973.1:c.9422G>T	XP_016865462.1:p.Gly3141Val
NR_003149.2:n.16320G>T