Canonical Allele Identifier: CA1562825024
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617837A= , CM000667.2:g.90617837A= GRCh38
NC_000005.9:g.89913654A= , CM000667.1:g.89913654A= GRCh37
NC_000005.8:g.89949410A= NCBI36
NG_007083.1:g.64038A=
NG_007083.2:g.93494A=

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.241A= MANE Select ENSP00000384582.2:p.Thr81=
ENST00000638316.1:n.451A=
ENST00000638638.1:n.648A=
ENST00000640109.1:n.337A=
ENST00000640281.1:n.300A=
ENST00000405460.6:c.241A= ENSP00000384582.2:p.Thr81=
ENST00000508842.5:c.253A= ENSP00000425936.1:p.Thr85=
NM_032119.3:c.241A= NP_115495.3:p.Thr81=
NR_003149.1:n.337A=
XM_011543675.1:c.241A= XP_011541977.1:p.Thr81=
XM_011543676.1:c.241A= XP_011541978.1:p.Thr81=
XM_011543678.1:c.241A= XP_011541980.1:p.Thr81=
XM_011543679.1:c.241A= XP_011541981.1:p.Thr81=
NM_032119.4:c.241A= MANE Select NP_115495.3:p.Thr81=
XM_017009963.2:c.241A= XP_016865452.1:p.Thr81=
XM_017009964.2:c.241A= XP_016865453.1:p.Thr81=
XM_017009965.1:c.238A= XP_016865454.1:p.Thr80=
XM_017009966.2:c.241A= XP_016865455.1:p.Thr81=
XM_017009967.1:c.241A= XP_016865456.1:p.Thr81=
XM_017009968.2:c.241A= XP_016865457.1:p.Thr81=
XM_017009969.2:c.241A= XP_016865458.1:p.Thr81=
XM_017009970.2:c.241A= XP_016865459.1:p.Thr81=
XM_017009971.2:c.241A= XP_016865460.1:p.Thr81=
XM_017009974.2:c.241A= XP_016865463.1:p.Thr81=
NR_003149.2:n.340A=