Canonical Allele Identifier: CA360367184

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050964A>T (hg19) ; chr5:g.90755147A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755147A>T , CM000667.2:g.90755147A>T	GRCh38
NC_000005.9:g.90050964A>T , CM000667.1:g.90050964A>T	GRCh37
NC_000005.8:g.90086720A>T	NCBI36
NG_007083.1:g.201348A>T
NG_007083.2:g.230804A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11542A>T MANE Select	ENSP00000384582.2:p.Asn3848Tyr
ENST00000425867.3:c.673A>T	ENSP00000392618.3:p.Asn225Tyr
ENST00000639431.1:c.265+78938A>T	ENSP00000491057.1:n.265+78938A>T
ENST00000640374.1:n.4686A>T
ENST00000640464.1:n.1961A>T
ENST00000405460.6:c.11542A>T	ENSP00000384582.2:p.Asn3848Tyr
ENST00000509621.1:c.4239A>T
NM_032119.3:c.11542A>T	NP_115495.3:p.Asn3848Tyr
NR_003149.1:n.11555A>T
XM_011543675.1:c.11539A>T	XP_011541977.1:p.Asn3847Tyr
XM_011543676.1:c.11461A>T	XP_011541978.1:p.Asn3821Tyr
XM_011543677.1:c.8845A>T	XP_011541979.1:p.Asn2949Tyr
XM_011543678.1:c.11542A>T	XP_011541980.1:p.Asn3848Tyr
NM_032119.4:c.11542A>T MANE Select	NP_115495.3:p.Asn3848Tyr
XM_017009963.2:c.11563A>T	XP_016865452.1:p.Asn3855Tyr
XM_017009964.2:c.11560A>T	XP_016865453.1:p.Asn3854Tyr
XM_017009965.1:c.11560A>T	XP_016865454.1:p.Asn3854Tyr
XM_017009966.2:c.11482A>T	XP_016865455.1:p.Asn3828Tyr
XM_017009967.1:c.11467A>T	XP_016865456.1:p.Asn3823Tyr
XM_017009968.2:c.11563A>T	XP_016865457.1:p.Asn3855Tyr
XM_017009969.2:c.11563A>T	XP_016865458.1:p.Asn3855Tyr
XM_017009970.2:c.11563A>T	XP_016865459.1:p.Asn3855Tyr
XM_017009971.2:c.11563A>T	XP_016865460.1:p.Asn3855Tyr
XM_017009972.1:c.4681A>T	XP_016865461.1:p.Asn1561Tyr
XM_017009973.1:c.4660A>T	XP_016865462.1:p.Asn1554Tyr
NR_003149.2:n.11558A>T