Canonical Allele Identifier: CA445465669
Gene: ADGRV1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.89923261A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627444A>T , CM000667.2:g.90627444A>T GRCh38
NC_000005.9:g.89923261A>T , CM000667.1:g.89923261A>T GRCh37
NC_000005.8:g.89959017A>T NCBI36
NG_007083.1:g.73645A>T
NG_007083.2:g.103101A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.906A>T MANE Select ENSP00000384582.2:p.Ser302=
ENST00000640083.1:n.611A>T
ENST00000640109.1:n.1002A>T
ENST00000640281.1:n.965A>T
ENST00000405460.6:c.906A>T ENSP00000384582.2:p.Ser302=
NM_032119.3:c.906A>T NP_115495.3:p.Ser302=
NR_003149.1:n.1002A>T
XM_011543675.1:c.906A>T XP_011541977.1:p.Ser302=
XM_011543676.1:c.906A>T XP_011541978.1:p.Ser302=
XM_011543678.1:c.906A>T XP_011541980.1:p.Ser302=
XM_011543679.1:c.906A>T XP_011541981.1:p.Ser302=
NM_032119.4:c.906A>T MANE Select NP_115495.3:p.Ser302=
XM_017009963.2:c.906A>T XP_016865452.1:p.Ser302=
XM_017009964.2:c.906A>T XP_016865453.1:p.Ser302=
XM_017009965.1:c.903A>T XP_016865454.1:p.Ser301=
XM_017009966.2:c.906A>T XP_016865455.1:p.Ser302=
XM_017009967.1:c.810A>T XP_016865456.1:p.Ser270=
XM_017009968.2:c.906A>T XP_016865457.1:p.Ser302=
XM_017009969.2:c.906A>T XP_016865458.1:p.Ser302=
XM_017009970.2:c.906A>T XP_016865459.1:p.Ser302=
XM_017009971.2:c.906A>T XP_016865460.1:p.Ser302=
XM_017009974.2:c.906A>T XP_016865463.1:p.Ser302=
NR_003149.2:n.1005A>T