Canonical Allele Identifier: CA360401736
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90791217T>A , CM000667.2:g.90791217T>A GRCh38
NC_000005.9:g.90087034T>A , CM000667.1:g.90087034T>A GRCh37
NC_000005.8:g.90122790T>A NCBI36
NG_007083.1:g.237418T>A
NG_007083.2:g.266874T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.14388T>A MANE Select ENSP00000384582.2:p.Asp4796Glu
ENST00000425867.3:c.3342T>A ENSP00000392618.3:p.Asp1114Glu
ENST00000507314.2:c.63T>A ENSP00000491299.1:p.Asp21Glu
ENST00000638510.1:n.1655T>A
ENST00000638585.1:n.154T>A
ENST00000638975.1:c.1017T>A ENSP00000492630.1:p.Asp339Glu
ENST00000639431.1:c.265+115008T>A ENSP00000491057.1:n.265+115008T>A
ENST00000640407.1:c.798T>A ENSP00000491425.1:p.Asp266Glu
ENST00000405460.6:c.14388T>A ENSP00000384582.2:p.Asp4796Glu
ENST00000425867.2:c.1371T>A ENSP00000392618.2:p.Asp457Glu
ENST00000507314.1:n.63T>A
NM_032119.3:c.14388T>A NP_115495.3:p.Asp4796Glu
NR_003149.1:n.14401T>A
XM_011543675.1:c.14385T>A XP_011541977.1:p.Asp4795Glu
XM_011543676.1:c.14307T>A XP_011541978.1:p.Asp4769Glu
XM_011543677.1:c.11691T>A XP_011541979.1:p.Asp3897Glu
XM_011543678.1:c.14388T>A XP_011541980.1:p.Asp4796Glu
NM_032119.4:c.14388T>A MANE Select NP_115495.3:p.Asp4796Glu
XM_017009963.2:c.14409T>A XP_016865452.1:p.Asp4803Glu
XM_017009964.2:c.14406T>A XP_016865453.1:p.Asp4802Glu
XM_017009965.1:c.14406T>A XP_016865454.1:p.Asp4802Glu
XM_017009966.2:c.14328T>A XP_016865455.1:p.Asp4776Glu
XM_017009967.1:c.14313T>A XP_016865456.1:p.Asp4771Glu
XM_017009968.2:c.14409T>A XP_016865457.1:p.Asp4803Glu
XM_017009969.2:c.14409T>A XP_016865458.1:p.Asp4803Glu
XM_017009970.2:c.14409T>A XP_016865459.1:p.Asp4803Glu
XM_017009971.2:c.14409T>A XP_016865460.1:p.Asp4803Glu
XM_017009972.1:c.7527T>A XP_016865461.1:p.Asp2509Glu
XM_017009973.1:c.7506T>A XP_016865462.1:p.Asp2502Glu
NR_003149.2:n.14404T>A