Canonical Allele Identifier: CA3340516
Community Standard Title: NM_032119.4(ADGRV1):c.9475A>G (p.Thr3159Ala)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90720075A>G , CM000667.2:g.90720075A>G GRCh38
NC_000005.9:g.90015892A>G , CM000667.1:g.90015892A>G GRCh37
NC_000005.8:g.90051648A>G NCBI36
NG_007083.1:g.166276A>G
NG_007083.2:g.195732A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.9475A>G MANE Select NP_115495.3:p.Thr3159Ala
ENST00000405460.9:c.9475A>G MANE Select ENSP00000384582.2:p.Thr3159Ala
NM_032119.3:c.9475A>G NP_115495.3:p.Thr3159Ala
NR_003149.1:n.9488A>G
NR_003149.2:n.9491A>G
ENST00000405460.6:c.9475A>G ENSP00000384582.2:p.Thr3159Ala
ENST00000509621.1:c.2172A>G
ENST00000639431.1:c.265+43866A>G ENSP00000491057.1:n.265+43866A>G
ENST00000640374.1:n.2619A>G
ENST00000640779.1:c.4204A>G
XM_011543675.1:c.9472A>G XP_011541977.1:p.Thr3158Ala
XM_011543676.1:c.9394A>G XP_011541978.1:p.Thr3132Ala
XM_011543677.1:c.6778A>G XP_011541979.1:p.Thr2260Ala
XM_011543678.1:c.9475A>G XP_011541980.1:p.Thr3159Ala
XM_011543679.1:c.9475A>G XP_011541981.1:p.Thr3159Ala
XM_017009963.2:c.9496A>G XP_016865452.1:p.Thr3166Ala
XM_017009964.2:c.9493A>G XP_016865453.1:p.Thr3165Ala
XM_017009965.1:c.9493A>G XP_016865454.1:p.Thr3165Ala
XM_017009966.2:c.9415A>G XP_016865455.1:p.Thr3139Ala
XM_017009967.1:c.9400A>G XP_016865456.1:p.Thr3134Ala
XM_017009968.2:c.9496A>G XP_016865457.1:p.Thr3166Ala
XM_017009969.2:c.9496A>G XP_016865458.1:p.Thr3166Ala
XM_017009970.2:c.9496A>G XP_016865459.1:p.Thr3166Ala
XM_017009971.2:c.9496A>G XP_016865460.1:p.Thr3166Ala
XM_017009972.1:c.2614A>G XP_016865461.1:p.Thr872Ala
XM_017009973.1:c.2593A>G XP_016865462.1:p.Thr865Ala
XM_017009974.2:c.9496A>G XP_016865463.1:p.Thr3166Ala
XR_001742802.1:n.2523-4266T>C
XR_948560.1:n.272-4266T>C