Canonical Allele Identifier: CA413475692
Community Standard Title: NM_004312.3(ARR3):c.298C>T (p.Arg100Ter)
Gene: ARR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70276234C>T , CM000685.2:g.70276234C>T GRCh38
NC_000023.10:g.69496084C>T , CM000685.1:g.69496084C>T GRCh37
NC_000023.9:g.69412809C>T NCBI36
NG_050734.1:g.17732C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004312.3:c.298C>T MANE Select NP_004303.2:p.Arg100Ter
ENST00000307959.9:c.298C>T MANE Select ENSP00000311538.8:p.Arg100Ter
NM_004312.2:c.298C>T NP_004303.2:p.Arg100Ter
ENST00000307959.8:c.298C>T ENSP00000311538.8:p.Arg100Ter
ENST00000374495.7:c.298C>T ENSP00000363619.3:p.Arg100Ter
ENST00000480877.6:c.145C>T ENSP00000425505.1:p.Arg49Ter
ENST00000620997.4:c.298C>T ENSP00000480426.1:p.Arg100Ter
XM_011530956.1:c.412C>T XP_011529258.1:p.Arg138Ter
XM_017029518.1:c.343C>T XP_016885007.1:p.Arg115Ter
XR_938428.1:n.503+4516G>A
XR_938429.1:n.503+4516G>A