Canonical Allele Identifier: CA360385530
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617885T>A , CM000667.2:g.90617885T>A GRCh38
NC_000005.9:g.89913702T>A , CM000667.1:g.89913702T>A GRCh37
NC_000005.8:g.89949458T>A NCBI36
NG_007083.1:g.64086T>A
NG_007083.2:g.93542T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.289T>A MANE Select ENSP00000384582.2:p.Tyr97Asn
ENST00000638316.1:n.499T>A
ENST00000638638.1:n.696T>A
ENST00000640109.1:n.385T>A
ENST00000640281.1:n.348T>A
ENST00000405460.6:c.289T>A ENSP00000384582.2:p.Tyr97Asn
ENST00000508842.5:c.301T>A ENSP00000425936.1:p.Tyr101Asn
NM_032119.3:c.289T>A NP_115495.3:p.Tyr97Asn
NR_003149.1:n.385T>A
XM_011543675.1:c.289T>A XP_011541977.1:p.Tyr97Asn
XM_011543676.1:c.289T>A XP_011541978.1:p.Tyr97Asn
XM_011543678.1:c.289T>A XP_011541980.1:p.Tyr97Asn
XM_011543679.1:c.289T>A XP_011541981.1:p.Tyr97Asn
NM_032119.4:c.289T>A MANE Select NP_115495.3:p.Tyr97Asn
XM_017009963.2:c.289T>A XP_016865452.1:p.Tyr97Asn
XM_017009964.2:c.289T>A XP_016865453.1:p.Tyr97Asn
XM_017009965.1:c.286T>A XP_016865454.1:p.Tyr96Asn
XM_017009966.2:c.289T>A XP_016865455.1:p.Tyr97Asn
XM_017009967.1:c.289T>A XP_016865456.1:p.Tyr97Asn
XM_017009968.2:c.289T>A XP_016865457.1:p.Tyr97Asn
XM_017009969.2:c.289T>A XP_016865458.1:p.Tyr97Asn
XM_017009970.2:c.289T>A XP_016865459.1:p.Tyr97Asn
XM_017009971.2:c.289T>A XP_016865460.1:p.Tyr97Asn
XM_017009974.2:c.289T>A XP_016865463.1:p.Tyr97Asn
NR_003149.2:n.388T>A