Canonical Allele Identifier: CA360366297

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050823C>T (hg19) ; chr5:g.90755006C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755006C>T , CM000667.2:g.90755006C>T	GRCh38
NC_000005.9:g.90050823C>T , CM000667.1:g.90050823C>T	GRCh37
NC_000005.8:g.90086579C>T	NCBI36
NG_007083.1:g.201207C>T
NG_007083.2:g.230663C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11401C>T MANE Select	ENSP00000384582.2:p.Gln3801Ter
ENST00000425867.3:c.532C>T	ENSP00000392618.3:p.Gln178Ter
ENST00000639431.1:c.265+78797C>T	ENSP00000491057.1:n.265+78797C>T
ENST00000640374.1:n.4545C>T
ENST00000640464.1:n.1820C>T
ENST00000405460.6:c.11401C>T	ENSP00000384582.2:p.Gln3801Ter
ENST00000509621.1:c.4098C>T
NM_032119.3:c.11401C>T	NP_115495.3:p.Gln3801Ter
NR_003149.1:n.11414C>T
XM_011543675.1:c.11398C>T	XP_011541977.1:p.Gln3800Ter
XM_011543676.1:c.11320C>T	XP_011541978.1:p.Gln3774Ter
XM_011543677.1:c.8704C>T	XP_011541979.1:p.Gln2902Ter
XM_011543678.1:c.11401C>T	XP_011541980.1:p.Gln3801Ter
NM_032119.4:c.11401C>T MANE Select	NP_115495.3:p.Gln3801Ter
XM_017009963.2:c.11422C>T	XP_016865452.1:p.Gln3808Ter
XM_017009964.2:c.11419C>T	XP_016865453.1:p.Gln3807Ter
XM_017009965.1:c.11419C>T	XP_016865454.1:p.Gln3807Ter
XM_017009966.2:c.11341C>T	XP_016865455.1:p.Gln3781Ter
XM_017009967.1:c.11326C>T	XP_016865456.1:p.Gln3776Ter
XM_017009968.2:c.11422C>T	XP_016865457.1:p.Gln3808Ter
XM_017009969.2:c.11422C>T	XP_016865458.1:p.Gln3808Ter
XM_017009970.2:c.11422C>T	XP_016865459.1:p.Gln3808Ter
XM_017009971.2:c.11422C>T	XP_016865460.1:p.Gln3808Ter
XM_017009972.1:c.4540C>T	XP_016865461.1:p.Gln1514Ter
XM_017009973.1:c.4519C>T	XP_016865462.1:p.Gln1507Ter
NR_003149.2:n.11417C>T