Canonical Allele Identifier: CA344879272
Community Standard Title: NM_001164688.2(RD3):c.238C>T (p.Gln80Ter)
Gene: RD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211481178G>A , CM000663.2:g.211481178G>A GRCh38
NC_000001.10:g.211654520G>A , CM000663.1:g.211654520G>A GRCh37
NC_000001.9:g.209721143G>A NCBI36
NG_013042.1:g.16740C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001164688.2:c.238C>T MANE Select NP_001158160.1:p.Gln80Ter
ENST00000680073.1:c.238C>T MANE Select ENSP00000505312.1:p.Gln80Ter
NM_001164688.1:c.238C>T NP_001158160.1:p.Gln80Ter
NM_183059.2:c.238C>T NP_898882.1:p.Gln80Ter
NM_183059.3:c.238C>T NP_898882.1:p.Gln80Ter
ENST00000367002.4:c.238C>T ENSP00000355969.4:p.Gln80Ter
ENST00000367002.5:c.238C>T ENSP00000355969.4:p.Gln80Ter
ENST00000484910.1:n.265-1851C>T
XM_011509479.1:c.238C>T XP_011507781.1:p.Gln80Ter
XM_017001151.1:c.274C>T XP_016856640.1:p.Gln92Ter