Canonical Allele Identifier: CA360407481

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90040880G>C (hg19) ; chr5:g.90745063G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745063G>C , CM000667.2:g.90745063G>C	GRCh38
NC_000005.9:g.90040880G>C , CM000667.1:g.90040880G>C	GRCh37
NC_000005.8:g.90076636G>C	NCBI36
NG_007083.1:g.191264G>C
NG_007083.2:g.220720G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10567G>C MANE Select	ENSP00000384582.2:p.Gly3523Arg
ENST00000639431.1:c.265+68854G>C	ENSP00000491057.1:n.265+68854G>C
ENST00000640374.1:n.3711G>C
ENST00000640464.1:n.986G>C
ENST00000405460.6:c.10567G>C	ENSP00000384582.2:p.Gly3523Arg
ENST00000509621.1:c.3264G>C
NM_032119.3:c.10567G>C	NP_115495.3:p.Gly3523Arg
NR_003149.1:n.10580G>C
XM_011543675.1:c.10564G>C	XP_011541977.1:p.Gly3522Arg
XM_011543676.1:c.10486G>C	XP_011541978.1:p.Gly3496Arg
XM_011543677.1:c.7870G>C	XP_011541979.1:p.Gly2624Arg
XM_011543678.1:c.10567G>C	XP_011541980.1:p.Gly3523Arg
XM_011543679.1:c.10567G>C	XP_011541981.1:p.Gly3523Arg
NM_032119.4:c.10567G>C MANE Select	NP_115495.3:p.Gly3523Arg
XM_017009963.2:c.10588G>C	XP_016865452.1:p.Gly3530Arg
XM_017009964.2:c.10585G>C	XP_016865453.1:p.Gly3529Arg
XM_017009965.1:c.10585G>C	XP_016865454.1:p.Gly3529Arg
XM_017009966.2:c.10507G>C	XP_016865455.1:p.Gly3503Arg
XM_017009967.1:c.10492G>C	XP_016865456.1:p.Gly3498Arg
XM_017009968.2:c.10588G>C	XP_016865457.1:p.Gly3530Arg
XM_017009969.2:c.10588G>C	XP_016865458.1:p.Gly3530Arg
XM_017009970.2:c.10588G>C	XP_016865459.1:p.Gly3530Arg
XM_017009971.2:c.10588G>C	XP_016865460.1:p.Gly3530Arg
XM_017009972.1:c.3706G>C	XP_016865461.1:p.Gly1236Arg
XM_017009973.1:c.3685G>C	XP_016865462.1:p.Gly1229Arg
XM_017009974.2:c.10588G>C	XP_016865463.1:p.Gly3530Arg
NR_003149.2:n.10583G>C