Canonical Allele Identifier: CA360410374

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106723A>G (hg19) ; chr5:g.90810906A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810906A>G , CM000667.2:g.90810906A>G	GRCh38
NC_000005.9:g.90106723A>G , CM000667.1:g.90106723A>G	GRCh37
NC_000005.8:g.90142479A>G	NCBI36
NG_007083.1:g.257107A>G
NG_007083.2:g.286563A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15646A>G MANE Select	ENSP00000384582.2:p.Ile5216Val
ENST00000425867.3:c.4600A>G	ENSP00000392618.3:p.Ile1534Val
ENST00000638510.1:n.2913A>G
ENST00000639431.1:c.265+134697A>G	ENSP00000491057.1:n.265+134697A>G
ENST00000640407.1:c.2056A>G	ENSP00000491425.1:p.Ile686Val
ENST00000405460.6:c.15646A>G	ENSP00000384582.2:p.Ile5216Val
ENST00000425867.2:c.2629A>G	ENSP00000392618.2:p.Ile877Val
NM_032119.3:c.15646A>G	NP_115495.3:p.Ile5216Val
NR_003149.1:n.15659A>G
XM_011543675.1:c.15643A>G	XP_011541977.1:p.Ile5215Val
XM_011543676.1:c.15565A>G	XP_011541978.1:p.Ile5189Val
XM_011543677.1:c.12949A>G	XP_011541979.1:p.Ile4317Val
NM_032119.4:c.15646A>G MANE Select	NP_115495.3:p.Ile5216Val
XM_017009963.2:c.15667A>G	XP_016865452.1:p.Ile5223Val
XM_017009964.2:c.15664A>G	XP_016865453.1:p.Ile5222Val
XM_017009965.1:c.15664A>G	XP_016865454.1:p.Ile5222Val
XM_017009966.2:c.15586A>G	XP_016865455.1:p.Ile5196Val
XM_017009967.1:c.15571A>G	XP_016865456.1:p.Ile5191Val
XM_017009968.2:c.15487A>G	XP_016865457.1:p.Ile5163Val
XM_017009969.2:c.15667A>G	XP_016865458.1:p.Ile5223Val
XM_017009972.1:c.8785A>G	XP_016865461.1:p.Ile2929Val
XM_017009973.1:c.8764A>G	XP_016865462.1:p.Ile2922Val
NR_003149.2:n.15662A>G