Canonical Allele Identifier: CA445465305
Community Standard Title: NM_032119.4(ADGRV1):c.1254A>G (p.Thr418=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90628577A>G , CM000667.2:g.90628577A>G GRCh38
NC_000005.9:g.89924394A>G , CM000667.1:g.89924394A>G GRCh37
NC_000005.8:g.89960150A>G NCBI36
NG_007083.1:g.74778A>G
NG_007083.2:g.104234A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.1254A>G MANE Select NP_115495.3:p.Thr418=
ENST00000405460.9:c.1254A>G MANE Select ENSP00000384582.2:p.Thr418=
NM_032119.3:c.1254A>G NP_115495.3:p.Thr418=
NR_003149.1:n.1350A>G
NR_003149.2:n.1353A>G
ENST00000405460.6:c.1254A>G ENSP00000384582.2:p.Thr418=
ENST00000504142.1:c.19A>G
ENST00000504142.2:n.20A>G
ENST00000640083.1:n.959A>G
ENST00000640109.1:n.1350A>G
XM_011543675.1:c.1254A>G XP_011541977.1:p.Thr418=
XM_011543676.1:c.1254A>G XP_011541978.1:p.Thr418=
XM_011543678.1:c.1254A>G XP_011541980.1:p.Thr418=
XM_011543679.1:c.1254A>G XP_011541981.1:p.Thr418=
XM_017009963.2:c.1254A>G XP_016865452.1:p.Thr418=
XM_017009964.2:c.1254A>G XP_016865453.1:p.Thr418=
XM_017009965.1:c.1251A>G XP_016865454.1:p.Thr417=
XM_017009966.2:c.1254A>G XP_016865455.1:p.Thr418=
XM_017009967.1:c.1158A>G XP_016865456.1:p.Thr386=
XM_017009968.2:c.1254A>G XP_016865457.1:p.Thr418=
XM_017009969.2:c.1254A>G XP_016865458.1:p.Thr418=
XM_017009970.2:c.1254A>G XP_016865459.1:p.Thr418=
XM_017009971.2:c.1254A>G XP_016865460.1:p.Thr418=
XM_017009974.2:c.1254A>G XP_016865463.1:p.Thr418=