Canonical Allele Identifier: CA360367453

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050994A>T (hg19) ; chr5:g.90755177A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755177A>T , CM000667.2:g.90755177A>T	GRCh38
NC_000005.9:g.90050994A>T , CM000667.1:g.90050994A>T	GRCh37
NC_000005.8:g.90086750A>T	NCBI36
NG_007083.1:g.201378A>T
NG_007083.2:g.230834A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11572A>T MANE Select	ENSP00000384582.2:p.Ile3858Phe
ENST00000425867.3:c.703A>T	ENSP00000392618.3:p.Ile235Phe
ENST00000639431.1:c.265+78968A>T	ENSP00000491057.1:n.265+78968A>T
ENST00000640374.1:n.4716A>T
ENST00000640464.1:n.1991A>T
ENST00000405460.6:c.11572A>T	ENSP00000384582.2:p.Ile3858Phe
ENST00000509621.1:c.4269A>T
NM_032119.3:c.11572A>T	NP_115495.3:p.Ile3858Phe
NR_003149.1:n.11585A>T
XM_011543675.1:c.11569A>T	XP_011541977.1:p.Ile3857Phe
XM_011543676.1:c.11491A>T	XP_011541978.1:p.Ile3831Phe
XM_011543677.1:c.8875A>T	XP_011541979.1:p.Ile2959Phe
XM_011543678.1:c.11572A>T	XP_011541980.1:p.Ile3858Phe
NM_032119.4:c.11572A>T MANE Select	NP_115495.3:p.Ile3858Phe
XM_017009963.2:c.11593A>T	XP_016865452.1:p.Ile3865Phe
XM_017009964.2:c.11590A>T	XP_016865453.1:p.Ile3864Phe
XM_017009965.1:c.11590A>T	XP_016865454.1:p.Ile3864Phe
XM_017009966.2:c.11512A>T	XP_016865455.1:p.Ile3838Phe
XM_017009967.1:c.11497A>T	XP_016865456.1:p.Ile3833Phe
XM_017009968.2:c.11593A>T	XP_016865457.1:p.Ile3865Phe
XM_017009969.2:c.11593A>T	XP_016865458.1:p.Ile3865Phe
XM_017009970.2:c.11593A>T	XP_016865459.1:p.Ile3865Phe
XM_017009971.2:c.11593A>T	XP_016865460.1:p.Ile3865Phe
XM_017009972.1:c.4711A>T	XP_016865461.1:p.Ile1571Phe
XM_017009973.1:c.4690A>T	XP_016865462.1:p.Ile1564Phe
NR_003149.2:n.11588A>T