Canonical Allele Identifier: CA3339026
Community Standard Title: NM_032119.4(ADGRV1):c.2820A>G (p.Val940=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90644791A>G , CM000667.2:g.90644791A>G GRCh38
NC_000005.9:g.89940608A>G , CM000667.1:g.89940608A>G GRCh37
NC_000005.8:g.89976364A>G NCBI36
NG_007083.1:g.90992A>G
NG_007083.2:g.120448A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.2820A>G MANE Select NP_115495.3:p.Val940=
ENST00000405460.9:c.2820A>G MANE Select ENSP00000384582.2:p.Val940=
NM_032119.3:c.2820A>G NP_115495.3:p.Val940=
NR_003149.1:n.2916A>G
NR_003149.2:n.2919A>G
ENST00000405460.6:c.2820A>G ENSP00000384582.2:p.Val940=
ENST00000504142.1:c.1585A>G
ENST00000504142.2:n.1586A>G
ENST00000639676.1:n.418A>G
ENST00000640403.1:c.123A>G ENSP00000492531.1:p.Val41=
XM_011543675.1:c.2820A>G XP_011541977.1:p.Val940=
XM_011543676.1:c.2820A>G XP_011541978.1:p.Val940=
XM_011543677.1:c.123A>G XP_011541979.1:p.Val41=
XM_011543678.1:c.2820A>G XP_011541980.1:p.Val940=
XM_011543679.1:c.2820A>G XP_011541981.1:p.Val940=
XM_017009963.2:c.2820A>G XP_016865452.1:p.Val940=
XM_017009964.2:c.2820A>G XP_016865453.1:p.Val940=
XM_017009965.1:c.2817A>G XP_016865454.1:p.Val939=
XM_017009966.2:c.2820A>G XP_016865455.1:p.Val940=
XM_017009967.1:c.2724A>G XP_016865456.1:p.Val908=
XM_017009968.2:c.2820A>G XP_016865457.1:p.Val940=
XM_017009969.2:c.2820A>G XP_016865458.1:p.Val940=
XM_017009970.2:c.2820A>G XP_016865459.1:p.Val940=
XM_017009971.2:c.2820A>G XP_016865460.1:p.Val940=
XM_017009974.2:c.2820A>G XP_016865463.1:p.Val940=