Canonical Allele Identifier: CA360409192

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041508C>G (hg19) ; chr5:g.90745691C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745691C>G , CM000667.2:g.90745691C>G	GRCh38
NC_000005.9:g.90041508C>G , CM000667.1:g.90041508C>G	GRCh37
NC_000005.8:g.90077264C>G	NCBI36
NG_007083.1:g.191892C>G
NG_007083.2:g.221348C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10870C>G MANE Select	ENSP00000384582.2:p.Gln3624Glu
ENST00000425867.3:c.1C>G	ENSP00000392618.3:p.Gln1Glu
ENST00000639431.1:c.265+69482C>G	ENSP00000491057.1:n.265+69482C>G
ENST00000640374.1:n.4014C>G
ENST00000640464.1:n.1289C>G
ENST00000405460.6:c.10870C>G	ENSP00000384582.2:p.Gln3624Glu
ENST00000509621.1:c.3567C>G
NM_032119.3:c.10870C>G	NP_115495.3:p.Gln3624Glu
NR_003149.1:n.10883C>G
XM_011543675.1:c.10867C>G	XP_011541977.1:p.Gln3623Glu
XM_011543676.1:c.10789C>G	XP_011541978.1:p.Gln3597Glu
XM_011543677.1:c.8173C>G	XP_011541979.1:p.Gln2725Glu
XM_011543678.1:c.10870C>G	XP_011541980.1:p.Gln3624Glu
NM_032119.4:c.10870C>G MANE Select	NP_115495.3:p.Gln3624Glu
XM_017009963.2:c.10891C>G	XP_016865452.1:p.Gln3631Glu
XM_017009964.2:c.10888C>G	XP_016865453.1:p.Gln3630Glu
XM_017009965.1:c.10888C>G	XP_016865454.1:p.Gln3630Glu
XM_017009966.2:c.10810C>G	XP_016865455.1:p.Gln3604Glu
XM_017009967.1:c.10795C>G	XP_016865456.1:p.Gln3599Glu
XM_017009968.2:c.10891C>G	XP_016865457.1:p.Gln3631Glu
XM_017009969.2:c.10891C>G	XP_016865458.1:p.Gln3631Glu
XM_017009970.2:c.10891C>G	XP_016865459.1:p.Gln3631Glu
XM_017009971.2:c.10891C>G	XP_016865460.1:p.Gln3631Glu
XM_017009972.1:c.4009C>G	XP_016865461.1:p.Gln1337Glu
XM_017009973.1:c.3988C>G	XP_016865462.1:p.Gln1330Glu
NR_003149.2:n.10886C>G