Canonical Allele Identifier: CA1562867517
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90712293C= , CM000667.2:g.90712293C= GRCh38
NC_000005.9:g.90008110C= , CM000667.1:g.90008110C= GRCh37
NC_000005.8:g.90043866C= NCBI36
NG_007083.1:g.158494C=
NG_007083.2:g.187950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9049C= MANE Select ENSP00000384582.2:p.His3017=
ENST00000639431.1:c.265+36084C= ENSP00000491057.1:n.265+36084C=
ENST00000639473.1:n.4508C=
ENST00000640012.1:c.2856C=
ENST00000640374.1:n.2193C=
ENST00000640779.1:c.3778C=
ENST00000405460.6:c.9049C= ENSP00000384582.2:p.His3017=
ENST00000509621.1:c.1746C=
NM_032119.3:c.9049C= NP_115495.3:p.His3017=
NR_003149.1:n.9062C=
XM_011543675.1:c.9046C= XP_011541977.1:p.His3016=
XM_011543676.1:c.8968C= XP_011541978.1:p.His2990=
XM_011543677.1:c.6352C= XP_011541979.1:p.His2118=
XM_011543678.1:c.9049C= XP_011541980.1:p.His3017=
XM_011543679.1:c.9049C= XP_011541981.1:p.His3017=
NM_032119.4:c.9049C= MANE Select NP_115495.3:p.His3017=
XM_017009963.2:c.9070C= XP_016865452.1:p.His3024=
XM_017009964.2:c.9067C= XP_016865453.1:p.His3023=
XM_017009965.1:c.9067C= XP_016865454.1:p.His3023=
XM_017009966.2:c.8989C= XP_016865455.1:p.His2997=
XM_017009967.1:c.8974C= XP_016865456.1:p.His2992=
XM_017009968.2:c.9070C= XP_016865457.1:p.His3024=
XM_017009969.2:c.9070C= XP_016865458.1:p.His3024=
XM_017009970.2:c.9070C= XP_016865459.1:p.His3024=
XM_017009971.2:c.9070C= XP_016865460.1:p.His3024=
XM_017009972.1:c.2188C= XP_016865461.1:p.His730=
XM_017009973.1:c.2167C= XP_016865462.1:p.His723=
XM_017009974.2:c.9070C= XP_016865463.1:p.His3024=
NR_003149.2:n.9065C=