Canonical Allele Identifier: CA1562829325
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627311A= , CM000667.2:g.90627311A= GRCh38
NC_000005.9:g.89923128A= , CM000667.1:g.89923128A= GRCh37
NC_000005.8:g.89958884A= NCBI36
NG_007083.1:g.73512A=
NG_007083.2:g.102968A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.773A= MANE Select ENSP00000384582.2:p.Lys258=
ENST00000640083.1:n.478A=
ENST00000640109.1:n.869A=
ENST00000640281.1:n.832A=
ENST00000405460.6:c.773A= ENSP00000384582.2:p.Lys258=
NM_032119.3:c.773A= NP_115495.3:p.Lys258=
NR_003149.1:n.869A=
XM_011543675.1:c.773A= XP_011541977.1:p.Lys258=
XM_011543676.1:c.773A= XP_011541978.1:p.Lys258=
XM_011543678.1:c.773A= XP_011541980.1:p.Lys258=
XM_011543679.1:c.773A= XP_011541981.1:p.Lys258=
NM_032119.4:c.773A= MANE Select NP_115495.3:p.Lys258=
XM_017009963.2:c.773A= XP_016865452.1:p.Lys258=
XM_017009964.2:c.773A= XP_016865453.1:p.Lys258=
XM_017009965.1:c.770A= XP_016865454.1:p.Lys257=
XM_017009966.2:c.773A= XP_016865455.1:p.Lys258=
XM_017009967.1:c.677A= XP_016865456.1:p.Lys226=
XM_017009968.2:c.773A= XP_016865457.1:p.Lys258=
XM_017009969.2:c.773A= XP_016865458.1:p.Lys258=
XM_017009970.2:c.773A= XP_016865459.1:p.Lys258=
XM_017009971.2:c.773A= XP_016865460.1:p.Lys258=
XM_017009974.2:c.773A= XP_016865463.1:p.Lys258=
NR_003149.2:n.872A=