Canonical Allele Identifier: CA445436616

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119401C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823584C>T , CM000667.2:g.90823584C>T	GRCh38
NC_000005.9:g.90119401C>T , CM000667.1:g.90119401C>T	GRCh37
NC_000005.8:g.90155157C>T	NCBI36
NG_007083.1:g.269785C>T
NG_007083.2:g.299241C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16356C>T MANE Select	ENSP00000384582.2:p.Leu5452=
ENST00000425867.3:c.5310C>T	ENSP00000392618.3:p.Leu1770=
ENST00000638510.1:n.3623C>T
ENST00000639431.1:c.265+147375C>T	ENSP00000491057.1:n.265+147375C>T
ENST00000640061.1:n.128+1402C>T
ENST00000640407.1:c.2766C>T	ENSP00000491425.1:p.Leu922=
ENST00000405460.6:c.16356C>T	ENSP00000384582.2:p.Leu5452=
ENST00000425867.2:c.3339C>T	ENSP00000392618.2:p.Leu1113=
NM_032119.3:c.16356C>T	NP_115495.3:p.Leu5452=
NR_003149.1:n.16369C>T
XM_011543675.1:c.16353C>T	XP_011541977.1:p.Leu5451=
XM_011543676.1:c.16275C>T	XP_011541978.1:p.Leu5425=
XM_011543677.1:c.13659C>T	XP_011541979.1:p.Leu4553=
NM_032119.4:c.16356C>T MANE Select	NP_115495.3:p.Leu5452=
XM_017009963.2:c.16377C>T	XP_016865452.1:p.Leu5459=
XM_017009964.2:c.16374C>T	XP_016865453.1:p.Leu5458=
XM_017009965.1:c.16374C>T	XP_016865454.1:p.Leu5458=
XM_017009966.2:c.16296C>T	XP_016865455.1:p.Leu5432=
XM_017009967.1:c.16281C>T	XP_016865456.1:p.Leu5427=
XM_017009968.2:c.16197C>T	XP_016865457.1:p.Leu5399=
XM_017009969.2:c.16377C>T	XP_016865458.1:p.Leu5459=
XM_017009972.1:c.9495C>T	XP_016865461.1:p.Leu3165=
XM_017009973.1:c.9474C>T	XP_016865462.1:p.Leu3158=
NR_003149.2:n.16372C>T