Canonical Allele Identifier: CA360425756

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119397A>G (hg19) ; chr5:g.90823580A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823580A>G , CM000667.2:g.90823580A>G	GRCh38
NC_000005.9:g.90119397A>G , CM000667.1:g.90119397A>G	GRCh37
NC_000005.8:g.90155153A>G	NCBI36
NG_007083.1:g.269781A>G
NG_007083.2:g.299237A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16352A>G MANE Select	ENSP00000384582.2:p.Glu5451Gly
ENST00000425867.3:c.5306A>G	ENSP00000392618.3:p.Glu1769Gly
ENST00000638510.1:n.3619A>G
ENST00000639431.1:c.265+147371A>G	ENSP00000491057.1:n.265+147371A>G
ENST00000640061.1:n.128+1398A>G
ENST00000640407.1:c.2762A>G	ENSP00000491425.1:p.Glu921Gly
ENST00000405460.6:c.16352A>G	ENSP00000384582.2:p.Glu5451Gly
ENST00000425867.2:c.3335A>G	ENSP00000392618.2:p.Glu1112Gly
NM_032119.3:c.16352A>G	NP_115495.3:p.Glu5451Gly
NR_003149.1:n.16365A>G
XM_011543675.1:c.16349A>G	XP_011541977.1:p.Glu5450Gly
XM_011543676.1:c.16271A>G	XP_011541978.1:p.Glu5424Gly
XM_011543677.1:c.13655A>G	XP_011541979.1:p.Glu4552Gly
NM_032119.4:c.16352A>G MANE Select	NP_115495.3:p.Glu5451Gly
XM_017009963.2:c.16373A>G	XP_016865452.1:p.Glu5458Gly
XM_017009964.2:c.16370A>G	XP_016865453.1:p.Glu5457Gly
XM_017009965.1:c.16370A>G	XP_016865454.1:p.Glu5457Gly
XM_017009966.2:c.16292A>G	XP_016865455.1:p.Glu5431Gly
XM_017009967.1:c.16277A>G	XP_016865456.1:p.Glu5426Gly
XM_017009968.2:c.16193A>G	XP_016865457.1:p.Glu5398Gly
XM_017009969.2:c.16373A>G	XP_016865458.1:p.Glu5458Gly
XM_017009972.1:c.9491A>G	XP_016865461.1:p.Glu3164Gly
XM_017009973.1:c.9470A>G	XP_016865462.1:p.Glu3157Gly
NR_003149.2:n.16368A>G