Canonical Allele Identifier: CA360366776

Gene: ADGRV1

Linked Data

• COSMIC: COSM6241083
• MyVariant Identifiers: chr5:g.90050898G>T (hg19) ; chr5:g.90755081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755081G>T , CM000667.2:g.90755081G>T	GRCh38
NC_000005.9:g.90050898G>T , CM000667.1:g.90050898G>T	GRCh37
NC_000005.8:g.90086654G>T	NCBI36
NG_007083.1:g.201282G>T
NG_007083.2:g.230738G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11476G>T MANE Select	ENSP00000384582.2:p.Val3826Phe
ENST00000425867.3:c.607G>T	ENSP00000392618.3:p.Val203Phe
ENST00000639431.1:c.265+78872G>T	ENSP00000491057.1:n.265+78872G>T
ENST00000640374.1:n.4620G>T
ENST00000640464.1:n.1895G>T
ENST00000405460.6:c.11476G>T	ENSP00000384582.2:p.Val3826Phe
ENST00000509621.1:c.4173G>T
NM_032119.3:c.11476G>T	NP_115495.3:p.Val3826Phe
NR_003149.1:n.11489G>T
XM_011543675.1:c.11473G>T	XP_011541977.1:p.Val3825Phe
XM_011543676.1:c.11395G>T	XP_011541978.1:p.Val3799Phe
XM_011543677.1:c.8779G>T	XP_011541979.1:p.Val2927Phe
XM_011543678.1:c.11476G>T	XP_011541980.1:p.Val3826Phe
NM_032119.4:c.11476G>T MANE Select	NP_115495.3:p.Val3826Phe
XM_017009963.2:c.11497G>T	XP_016865452.1:p.Val3833Phe
XM_017009964.2:c.11494G>T	XP_016865453.1:p.Val3832Phe
XM_017009965.1:c.11494G>T	XP_016865454.1:p.Val3832Phe
XM_017009966.2:c.11416G>T	XP_016865455.1:p.Val3806Phe
XM_017009967.1:c.11401G>T	XP_016865456.1:p.Val3801Phe
XM_017009968.2:c.11497G>T	XP_016865457.1:p.Val3833Phe
XM_017009969.2:c.11497G>T	XP_016865458.1:p.Val3833Phe
XM_017009970.2:c.11497G>T	XP_016865459.1:p.Val3833Phe
XM_017009971.2:c.11497G>T	XP_016865460.1:p.Val3833Phe
XM_017009972.1:c.4615G>T	XP_016865461.1:p.Val1539Phe
XM_017009973.1:c.4594G>T	XP_016865462.1:p.Val1532Phe
NR_003149.2:n.11492G>T