Canonical Allele Identifier: CA360368347
Community Standard Title: NM_032119.4(ADGRV1):c.6852C>A (p.Asp2284Glu)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90690942C>A , CM000667.2:g.90690942C>A GRCh38
NC_000005.9:g.89986759C>A , CM000667.1:g.89986759C>A GRCh37
NC_000005.8:g.90022515C>A NCBI36
NG_007083.1:g.137143C>A
NG_007083.2:g.166599C>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.6852C>A MANE Select NP_115495.3:p.Asp2284Glu
ENST00000405460.9:c.6852C>A MANE Select ENSP00000384582.2:p.Asp2284Glu
NM_032119.3:c.6852C>A NP_115495.3:p.Asp2284Glu
NR_003149.1:n.6948C>A
NR_003149.2:n.6951C>A
ENST00000405460.6:c.6852C>A ENSP00000384582.2:p.Asp2284Glu
ENST00000639431.1:c.265+14733C>A ENSP00000491057.1:n.265+14733C>A
ENST00000639473.1:n.2311C>A
ENST00000640012.1:c.742C>A
ENST00000640403.1:c.4143C>A ENSP00000492531.1:p.Asp1381Glu
ENST00000640779.1:c.1664C>A
XM_011543675.1:c.6849C>A XP_011541977.1:p.Asp2283Glu
XM_011543676.1:c.6771C>A XP_011541978.1:p.Asp2257Glu
XM_011543677.1:c.4155C>A XP_011541979.1:p.Asp1385Glu
XM_011543678.1:c.6852C>A XP_011541980.1:p.Asp2284Glu
XM_011543679.1:c.6852C>A XP_011541981.1:p.Asp2284Glu
XM_017009963.2:c.6852C>A XP_016865452.1:p.Asp2284Glu
XM_017009964.2:c.6849C>A XP_016865453.1:p.Asp2283Glu
XM_017009965.1:c.6849C>A XP_016865454.1:p.Asp2283Glu
XM_017009966.2:c.6771C>A XP_016865455.1:p.Asp2257Glu
XM_017009967.1:c.6756C>A XP_016865456.1:p.Asp2252Glu
XM_017009968.2:c.6852C>A XP_016865457.1:p.Asp2284Glu
XM_017009969.2:c.6852C>A XP_016865458.1:p.Asp2284Glu
XM_017009970.2:c.6852C>A XP_016865459.1:p.Asp2284Glu
XM_017009971.2:c.6852C>A XP_016865460.1:p.Asp2284Glu
XM_017009972.1:c.53C>A XP_016865461.1:p.Thr18Asn
XM_017009973.1:c.53C>A XP_016865462.1:p.Thr18Asn
XM_017009974.2:c.6852C>A XP_016865463.1:p.Asp2284Glu