Canonical Allele Identifier: CA445465644

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89923222C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627405C>T , CM000667.2:g.90627405C>T	GRCh38
NC_000005.9:g.89923222C>T , CM000667.1:g.89923222C>T	GRCh37
NC_000005.8:g.89958978C>T	NCBI36
NG_007083.1:g.73606C>T
NG_007083.2:g.103062C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.867C>T MANE Select	ENSP00000384582.2:p.Asn289=
ENST00000640083.1:n.572C>T
ENST00000640109.1:n.963C>T
ENST00000640281.1:n.926C>T
ENST00000405460.6:c.867C>T	ENSP00000384582.2:p.Asn289=
NM_032119.3:c.867C>T	NP_115495.3:p.Asn289=
NR_003149.1:n.963C>T
XM_011543675.1:c.867C>T	XP_011541977.1:p.Asn289=
XM_011543676.1:c.867C>T	XP_011541978.1:p.Asn289=
XM_011543678.1:c.867C>T	XP_011541980.1:p.Asn289=
XM_011543679.1:c.867C>T	XP_011541981.1:p.Asn289=
NM_032119.4:c.867C>T MANE Select	NP_115495.3:p.Asn289=
XM_017009963.2:c.867C>T	XP_016865452.1:p.Asn289=
XM_017009964.2:c.867C>T	XP_016865453.1:p.Asn289=
XM_017009965.1:c.864C>T	XP_016865454.1:p.Asn288=
XM_017009966.2:c.867C>T	XP_016865455.1:p.Asn289=
XM_017009967.1:c.771C>T	XP_016865456.1:p.Asn257=
XM_017009968.2:c.867C>T	XP_016865457.1:p.Asn289=
XM_017009969.2:c.867C>T	XP_016865458.1:p.Asn289=
XM_017009970.2:c.867C>T	XP_016865459.1:p.Asn289=
XM_017009971.2:c.867C>T	XP_016865460.1:p.Asn289=
XM_017009974.2:c.867C>T	XP_016865463.1:p.Asn289=
NR_003149.2:n.966C>T