Canonical Allele Identifier: CA360367014

Gene: ADGRV1

Linked Data

• dbSNP Id: rs756810095
• MyVariant Identifiers: chr5:g.90050931G>T (hg19) ; chr5:g.90755114G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755114G>T , CM000667.2:g.90755114G>T	GRCh38
NC_000005.9:g.90050931G>T , CM000667.1:g.90050931G>T	GRCh37
NC_000005.8:g.90086687G>T	NCBI36
NG_007083.1:g.201315G>T
NG_007083.2:g.230771G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11509G>T MANE Select	ENSP00000384582.2:p.Val3837Leu
ENST00000425867.3:c.640G>T	ENSP00000392618.3:p.Val214Leu
ENST00000639431.1:c.265+78905G>T	ENSP00000491057.1:n.265+78905G>T
ENST00000640374.1:n.4653G>T
ENST00000640464.1:n.1928G>T
ENST00000405460.6:c.11509G>T	ENSP00000384582.2:p.Val3837Leu
ENST00000509621.1:c.4206G>T
NM_032119.3:c.11509G>T	NP_115495.3:p.Val3837Leu
NR_003149.1:n.11522G>T
XM_011543675.1:c.11506G>T	XP_011541977.1:p.Val3836Leu
XM_011543676.1:c.11428G>T	XP_011541978.1:p.Val3810Leu
XM_011543677.1:c.8812G>T	XP_011541979.1:p.Val2938Leu
XM_011543678.1:c.11509G>T	XP_011541980.1:p.Val3837Leu
NM_032119.4:c.11509G>T MANE Select	NP_115495.3:p.Val3837Leu
XM_017009963.2:c.11530G>T	XP_016865452.1:p.Val3844Leu
XM_017009964.2:c.11527G>T	XP_016865453.1:p.Val3843Leu
XM_017009965.1:c.11527G>T	XP_016865454.1:p.Val3843Leu
XM_017009966.2:c.11449G>T	XP_016865455.1:p.Val3817Leu
XM_017009967.1:c.11434G>T	XP_016865456.1:p.Val3812Leu
XM_017009968.2:c.11530G>T	XP_016865457.1:p.Val3844Leu
XM_017009969.2:c.11530G>T	XP_016865458.1:p.Val3844Leu
XM_017009970.2:c.11530G>T	XP_016865459.1:p.Val3844Leu
XM_017009971.2:c.11530G>T	XP_016865460.1:p.Val3844Leu
XM_017009972.1:c.4648G>T	XP_016865461.1:p.Val1550Leu
XM_017009973.1:c.4627G>T	XP_016865462.1:p.Val1543Leu
NR_003149.2:n.11525G>T