Canonical Allele Identifier: CA445436576

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119335T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823518T>G , CM000667.2:g.90823518T>G	GRCh38
NC_000005.9:g.90119335T>G , CM000667.1:g.90119335T>G	GRCh37
NC_000005.8:g.90155091T>G	NCBI36
NG_007083.1:g.269719T>G
NG_007083.2:g.299175T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16290T>G MANE Select	ENSP00000384582.2:p.Leu5430=
ENST00000425867.3:c.5244T>G	ENSP00000392618.3:p.Leu1748=
ENST00000638510.1:n.3557T>G
ENST00000639431.1:c.265+147309T>G	ENSP00000491057.1:n.265+147309T>G
ENST00000640061.1:n.128+1336T>G
ENST00000640407.1:c.2700T>G	ENSP00000491425.1:p.Leu900=
ENST00000405460.6:c.16290T>G	ENSP00000384582.2:p.Leu5430=
ENST00000425867.2:c.3273T>G	ENSP00000392618.2:p.Leu1091=
NM_032119.3:c.16290T>G	NP_115495.3:p.Leu5430=
NR_003149.1:n.16303T>G
XM_011543675.1:c.16287T>G	XP_011541977.1:p.Leu5429=
XM_011543676.1:c.16209T>G	XP_011541978.1:p.Leu5403=
XM_011543677.1:c.13593T>G	XP_011541979.1:p.Leu4531=
NM_032119.4:c.16290T>G MANE Select	NP_115495.3:p.Leu5430=
XM_017009963.2:c.16311T>G	XP_016865452.1:p.Leu5437=
XM_017009964.2:c.16308T>G	XP_016865453.1:p.Leu5436=
XM_017009965.1:c.16308T>G	XP_016865454.1:p.Leu5436=
XM_017009966.2:c.16230T>G	XP_016865455.1:p.Leu5410=
XM_017009967.1:c.16215T>G	XP_016865456.1:p.Leu5405=
XM_017009968.2:c.16131T>G	XP_016865457.1:p.Leu5377=
XM_017009969.2:c.16311T>G	XP_016865458.1:p.Leu5437=
XM_017009972.1:c.9429T>G	XP_016865461.1:p.Leu3143=
XM_017009973.1:c.9408T>G	XP_016865462.1:p.Leu3136=
NR_003149.2:n.16306T>G