Canonical Allele Identifier: CA360366779

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11476G>C MANE Select	ENSP00000384582.2:p.Val3826Leu
ENST00000425867.3:c.607G>C	ENSP00000392618.3:p.Val203Leu
ENST00000639431.1:c.265+78872G>C	ENSP00000491057.1:n.265+78872G>C
ENST00000640374.1:n.4620G>C
ENST00000640464.1:n.1895G>C
ENST00000405460.6:c.11476G>C	ENSP00000384582.2:p.Val3826Leu
ENST00000509621.1:c.4173G>C
NM_032119.3:c.11476G>C	NP_115495.3:p.Val3826Leu
NR_003149.1:n.11489G>C
XM_011543675.1:c.11473G>C	XP_011541977.1:p.Val3825Leu
XM_011543676.1:c.11395G>C	XP_011541978.1:p.Val3799Leu
XM_011543677.1:c.8779G>C	XP_011541979.1:p.Val2927Leu
XM_011543678.1:c.11476G>C	XP_011541980.1:p.Val3826Leu
NM_032119.4:c.11476G>C MANE Select	NP_115495.3:p.Val3826Leu
XM_017009963.2:c.11497G>C	XP_016865452.1:p.Val3833Leu
XM_017009964.2:c.11494G>C	XP_016865453.1:p.Val3832Leu
XM_017009965.1:c.11494G>C	XP_016865454.1:p.Val3832Leu
XM_017009966.2:c.11416G>C	XP_016865455.1:p.Val3806Leu
XM_017009967.1:c.11401G>C	XP_016865456.1:p.Val3801Leu
XM_017009968.2:c.11497G>C	XP_016865457.1:p.Val3833Leu
XM_017009969.2:c.11497G>C	XP_016865458.1:p.Val3833Leu
XM_017009970.2:c.11497G>C	XP_016865459.1:p.Val3833Leu
XM_017009971.2:c.11497G>C	XP_016865460.1:p.Val3833Leu
XM_017009972.1:c.4615G>C	XP_016865461.1:p.Val1539Leu
XM_017009973.1:c.4594G>C	XP_016865462.1:p.Val1532Leu
NR_003149.2:n.11492G>C