Canonical Allele Identifier: CA360414021
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90683971C>A , CM000667.2:g.90683971C>A GRCh38
NC_000005.9:g.89979788C>A , CM000667.1:g.89979788C>A GRCh37
NC_000005.8:g.90015544C>A NCBI36
NG_007083.1:g.130172C>A
NG_007083.2:g.159628C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.6050C>A MANE Select ENSP00000384582.2:p.Thr2017Lys
ENST00000639431.1:c.265+7762C>A ENSP00000491057.1:n.265+7762C>A
ENST00000639473.1:n.1509C>A
ENST00000640012.1:c.165-1809C>A
ENST00000640403.1:c.3341C>A ENSP00000492531.1:p.Thr1114Lys
ENST00000640779.1:c.862C>A
ENST00000405460.6:c.6050C>A ENSP00000384582.2:p.Thr2017Lys
NM_032119.3:c.6050C>A NP_115495.3:p.Thr2017Lys
NR_003149.1:n.6146C>A
XM_011543675.1:c.6047C>A XP_011541977.1:p.Thr2016Lys
XM_011543676.1:c.5969C>A XP_011541978.1:p.Thr1990Lys
XM_011543677.1:c.3353C>A XP_011541979.1:p.Thr1118Lys
XM_011543678.1:c.6050C>A XP_011541980.1:p.Thr2017Lys
XM_011543679.1:c.6050C>A XP_011541981.1:p.Thr2017Lys
NM_032119.4:c.6050C>A MANE Select NP_115495.3:p.Thr2017Lys
XM_017009963.2:c.6050C>A XP_016865452.1:p.Thr2017Lys
XM_017009964.2:c.6047C>A XP_016865453.1:p.Thr2016Lys
XM_017009965.1:c.6047C>A XP_016865454.1:p.Thr2016Lys
XM_017009966.2:c.5969C>A XP_016865455.1:p.Thr1990Lys
XM_017009967.1:c.5954C>A XP_016865456.1:p.Thr1985Lys
XM_017009968.2:c.6050C>A XP_016865457.1:p.Thr2017Lys
XM_017009969.2:c.6050C>A XP_016865458.1:p.Thr2017Lys
XM_017009970.2:c.6050C>A XP_016865459.1:p.Thr2017Lys
XM_017009971.2:c.6050C>A XP_016865460.1:p.Thr2017Lys
XM_017009973.1:c.-750C>A XP_016865462.1:n.-750C>A
XM_017009974.2:c.6050C>A XP_016865463.1:p.Thr2017Lys
NR_003149.2:n.6149C>A