Canonical Allele Identifier: CA360409039

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041473A>G (hg19) ; chr5:g.90745656A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745656A>G , CM000667.2:g.90745656A>G	GRCh38
NC_000005.9:g.90041473A>G , CM000667.1:g.90041473A>G	GRCh37
NC_000005.8:g.90077229A>G	NCBI36
NG_007083.1:g.191857A>G
NG_007083.2:g.221313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10835A>G MANE Select	ENSP00000384582.2:p.Asp3612Gly
ENST00000639431.1:c.265+69447A>G	ENSP00000491057.1:n.265+69447A>G
ENST00000640374.1:n.3979A>G
ENST00000640464.1:n.1254A>G
ENST00000405460.6:c.10835A>G	ENSP00000384582.2:p.Asp3612Gly
ENST00000509621.1:c.3532A>G
NM_032119.3:c.10835A>G	NP_115495.3:p.Asp3612Gly
NR_003149.1:n.10848A>G
XM_011543675.1:c.10832A>G	XP_011541977.1:p.Asp3611Gly
XM_011543676.1:c.10754A>G	XP_011541978.1:p.Asp3585Gly
XM_011543677.1:c.8138A>G	XP_011541979.1:p.Asp2713Gly
XM_011543678.1:c.10835A>G	XP_011541980.1:p.Asp3612Gly
XM_011543679.1:c.*57A>G	XP_011541981.1:n.*57A>G
NM_032119.4:c.10835A>G MANE Select	NP_115495.3:p.Asp3612Gly
XM_017009963.2:c.10856A>G	XP_016865452.1:p.Asp3619Gly
XM_017009964.2:c.10853A>G	XP_016865453.1:p.Asp3618Gly
XM_017009965.1:c.10853A>G	XP_016865454.1:p.Asp3618Gly
XM_017009966.2:c.10775A>G	XP_016865455.1:p.Asp3592Gly
XM_017009967.1:c.10760A>G	XP_016865456.1:p.Asp3587Gly
XM_017009968.2:c.10856A>G	XP_016865457.1:p.Asp3619Gly
XM_017009969.2:c.10856A>G	XP_016865458.1:p.Asp3619Gly
XM_017009970.2:c.10856A>G	XP_016865459.1:p.Asp3619Gly
XM_017009971.2:c.10856A>G	XP_016865460.1:p.Asp3619Gly
XM_017009972.1:c.3974A>G	XP_016865461.1:p.Asp1325Gly
XM_017009973.1:c.3953A>G	XP_016865462.1:p.Asp1318Gly
XM_017009974.2:c.*57A>G	XP_016865463.1:n.*57A>G
NR_003149.2:n.10851A>G