Canonical Allele Identifier: CA360366977

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050928T>A (hg19) ; chr5:g.90755111T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755111T>A , CM000667.2:g.90755111T>A	GRCh38
NC_000005.9:g.90050928T>A , CM000667.1:g.90050928T>A	GRCh37
NC_000005.8:g.90086684T>A	NCBI36
NG_007083.1:g.201312T>A
NG_007083.2:g.230768T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11506T>A MANE Select	ENSP00000384582.2:p.Tyr3836Asn
ENST00000425867.3:c.637T>A	ENSP00000392618.3:p.Tyr213Asn
ENST00000639431.1:c.265+78902T>A	ENSP00000491057.1:n.265+78902T>A
ENST00000640374.1:n.4650T>A
ENST00000640464.1:n.1925T>A
ENST00000405460.6:c.11506T>A	ENSP00000384582.2:p.Tyr3836Asn
ENST00000509621.1:c.4203T>A
NM_032119.3:c.11506T>A	NP_115495.3:p.Tyr3836Asn
NR_003149.1:n.11519T>A
XM_011543675.1:c.11503T>A	XP_011541977.1:p.Tyr3835Asn
XM_011543676.1:c.11425T>A	XP_011541978.1:p.Tyr3809Asn
XM_011543677.1:c.8809T>A	XP_011541979.1:p.Tyr2937Asn
XM_011543678.1:c.11506T>A	XP_011541980.1:p.Tyr3836Asn
NM_032119.4:c.11506T>A MANE Select	NP_115495.3:p.Tyr3836Asn
XM_017009963.2:c.11527T>A	XP_016865452.1:p.Tyr3843Asn
XM_017009964.2:c.11524T>A	XP_016865453.1:p.Tyr3842Asn
XM_017009965.1:c.11524T>A	XP_016865454.1:p.Tyr3842Asn
XM_017009966.2:c.11446T>A	XP_016865455.1:p.Tyr3816Asn
XM_017009967.1:c.11431T>A	XP_016865456.1:p.Tyr3811Asn
XM_017009968.2:c.11527T>A	XP_016865457.1:p.Tyr3843Asn
XM_017009969.2:c.11527T>A	XP_016865458.1:p.Tyr3843Asn
XM_017009970.2:c.11527T>A	XP_016865459.1:p.Tyr3843Asn
XM_017009971.2:c.11527T>A	XP_016865460.1:p.Tyr3843Asn
XM_017009972.1:c.4645T>A	XP_016865461.1:p.Tyr1549Asn
XM_017009973.1:c.4624T>A	XP_016865462.1:p.Tyr1542Asn
NR_003149.2:n.11522T>A