Canonical Allele Identifier: CA445465662

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89923246T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627429T>C , CM000667.2:g.90627429T>C	GRCh38
NC_000005.9:g.89923246T>C , CM000667.1:g.89923246T>C	GRCh37
NC_000005.8:g.89959002T>C	NCBI36
NG_007083.1:g.73630T>C
NG_007083.2:g.103086T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.891T>C MANE Select	ENSP00000384582.2:p.Asp297=
ENST00000640083.1:n.596T>C
ENST00000640109.1:n.987T>C
ENST00000640281.1:n.950T>C
ENST00000405460.6:c.891T>C	ENSP00000384582.2:p.Asp297=
NM_032119.3:c.891T>C	NP_115495.3:p.Asp297=
NR_003149.1:n.987T>C
XM_011543675.1:c.891T>C	XP_011541977.1:p.Asp297=
XM_011543676.1:c.891T>C	XP_011541978.1:p.Asp297=
XM_011543678.1:c.891T>C	XP_011541980.1:p.Asp297=
XM_011543679.1:c.891T>C	XP_011541981.1:p.Asp297=
NM_032119.4:c.891T>C MANE Select	NP_115495.3:p.Asp297=
XM_017009963.2:c.891T>C	XP_016865452.1:p.Asp297=
XM_017009964.2:c.891T>C	XP_016865453.1:p.Asp297=
XM_017009965.1:c.888T>C	XP_016865454.1:p.Asp296=
XM_017009966.2:c.891T>C	XP_016865455.1:p.Asp297=
XM_017009967.1:c.795T>C	XP_016865456.1:p.Asp265=
XM_017009968.2:c.891T>C	XP_016865457.1:p.Asp297=
XM_017009969.2:c.891T>C	XP_016865458.1:p.Asp297=
XM_017009970.2:c.891T>C	XP_016865459.1:p.Asp297=
XM_017009971.2:c.891T>C	XP_016865460.1:p.Asp297=
XM_017009974.2:c.891T>C	XP_016865463.1:p.Asp297=
NR_003149.2:n.990T>C