Canonical Allele Identifier: CA360366917

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050919A>T (hg19) ; chr5:g.90755102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755102A>T , CM000667.2:g.90755102A>T	GRCh38
NC_000005.9:g.90050919A>T , CM000667.1:g.90050919A>T	GRCh37
NC_000005.8:g.90086675A>T	NCBI36
NG_007083.1:g.201303A>T
NG_007083.2:g.230759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11497A>T MANE Select	ENSP00000384582.2:p.Asn3833Tyr
ENST00000425867.3:c.628A>T	ENSP00000392618.3:p.Asn210Tyr
ENST00000639431.1:c.265+78893A>T	ENSP00000491057.1:n.265+78893A>T
ENST00000640374.1:n.4641A>T
ENST00000640464.1:n.1916A>T
ENST00000405460.6:c.11497A>T	ENSP00000384582.2:p.Asn3833Tyr
ENST00000509621.1:c.4194A>T
NM_032119.3:c.11497A>T	NP_115495.3:p.Asn3833Tyr
NR_003149.1:n.11510A>T
XM_011543675.1:c.11494A>T	XP_011541977.1:p.Asn3832Tyr
XM_011543676.1:c.11416A>T	XP_011541978.1:p.Asn3806Tyr
XM_011543677.1:c.8800A>T	XP_011541979.1:p.Asn2934Tyr
XM_011543678.1:c.11497A>T	XP_011541980.1:p.Asn3833Tyr
NM_032119.4:c.11497A>T MANE Select	NP_115495.3:p.Asn3833Tyr
XM_017009963.2:c.11518A>T	XP_016865452.1:p.Asn3840Tyr
XM_017009964.2:c.11515A>T	XP_016865453.1:p.Asn3839Tyr
XM_017009965.1:c.11515A>T	XP_016865454.1:p.Asn3839Tyr
XM_017009966.2:c.11437A>T	XP_016865455.1:p.Asn3813Tyr
XM_017009967.1:c.11422A>T	XP_016865456.1:p.Asn3808Tyr
XM_017009968.2:c.11518A>T	XP_016865457.1:p.Asn3840Tyr
XM_017009969.2:c.11518A>T	XP_016865458.1:p.Asn3840Tyr
XM_017009970.2:c.11518A>T	XP_016865459.1:p.Asn3840Tyr
XM_017009971.2:c.11518A>T	XP_016865460.1:p.Asn3840Tyr
XM_017009972.1:c.4636A>T	XP_016865461.1:p.Asn1546Tyr
XM_017009973.1:c.4615A>T	XP_016865462.1:p.Asn1539Tyr
NR_003149.2:n.11513A>T