Canonical Allele Identifier: CA360404426
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90728876G>A , CM000667.2:g.90728876G>A GRCh38
NC_000005.9:g.90024693G>A , CM000667.1:g.90024693G>A GRCh37
NC_000005.8:g.90060449G>A NCBI36
NG_007083.1:g.175077G>A
NG_007083.2:g.204533G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10369G>A MANE Select ENSP00000384582.2:p.Glu3457Lys
ENST00000639431.1:c.265+52667G>A ENSP00000491057.1:n.265+52667G>A
ENST00000640374.1:n.3513G>A
ENST00000640464.1:n.788G>A
ENST00000405460.6:c.10369G>A ENSP00000384582.2:p.Glu3457Lys
ENST00000509621.1:c.3066G>A
NM_032119.3:c.10369G>A NP_115495.3:p.Glu3457Lys
NR_003149.1:n.10382G>A
XM_011543675.1:c.10366G>A XP_011541977.1:p.Glu3456Lys
XM_011543676.1:c.10288G>A XP_011541978.1:p.Glu3430Lys
XM_011543677.1:c.7672G>A XP_011541979.1:p.Glu2558Lys
XM_011543678.1:c.10369G>A XP_011541980.1:p.Glu3457Lys
XM_011543679.1:c.10369G>A XP_011541981.1:p.Glu3457Lys
XR_948560.1:n.271+12031C>T
NM_032119.4:c.10369G>A MANE Select NP_115495.3:p.Glu3457Lys
XM_017009963.2:c.10390G>A XP_016865452.1:p.Glu3464Lys
XM_017009964.2:c.10387G>A XP_016865453.1:p.Glu3463Lys
XM_017009965.1:c.10387G>A XP_016865454.1:p.Glu3463Lys
XM_017009966.2:c.10309G>A XP_016865455.1:p.Glu3437Lys
XM_017009967.1:c.10294G>A XP_016865456.1:p.Glu3432Lys
XM_017009968.2:c.10390G>A XP_016865457.1:p.Glu3464Lys
XM_017009969.2:c.10390G>A XP_016865458.1:p.Glu3464Lys
XM_017009970.2:c.10390G>A XP_016865459.1:p.Glu3464Lys
XM_017009971.2:c.10390G>A XP_016865460.1:p.Glu3464Lys
XM_017009972.1:c.3508G>A XP_016865461.1:p.Glu1170Lys
XM_017009973.1:c.3487G>A XP_016865462.1:p.Glu1163Lys
XM_017009974.2:c.10390G>A XP_016865463.1:p.Glu3464Lys
XR_001742802.1:n.2522+12031C>T
NR_003149.2:n.10385G>A