Canonical Allele Identifier: CA382741844
Community Standard Title: NM_014956.5(CEP164):c.1408A>T (p.Arg470Trp)
Gene: CEP164 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.117380704A>T , CM000673.2:g.117380704A>T GRCh38
NC_000011.9:g.117251420A>T , CM000673.1:g.117251420A>T GRCh37
NC_000011.8:g.116756630A>T NCBI36
NG_033032.1:g.63927A>T

Transcript Alleles

HGVS Amino-acid Change
NM_014956.5:c.1408A>T MANE Select NP_055771.4:p.Arg470Trp
ENST00000278935.8:c.1408A>T MANE Select ENSP00000278935.3:p.Arg470Trp
NM_001271933.1:c.1408A>T NP_001258862.1:p.Arg470Trp
NM_001271933.2:c.1408A>T NP_001258862.1:p.Arg470Trp
NM_014956.4:c.1408A>T NP_055771.4:p.Arg470Trp
ENST00000278935.7:c.1408A>T ENSP00000278935.3:p.Arg470Trp
ENST00000533675.5:n.1654A>T
ENST00000533706.5:n.732A>T
XM_005271453.1:c.3094A>T XP_005271510.1:p.Arg1032Trp
XM_005271456.1:c.1408A>T XP_005271513.1:p.Arg470Trp
XM_005271457.1:c.1408A>T XP_005271514.1:p.Arg470Trp
XM_006718788.1:c.3094A>T XP_006718851.1:p.Arg1032Trp
XM_006718794.1:c.1330A>T XP_006718857.1:p.Arg444Trp
XM_011542670.1:c.3094A>T XP_011540972.1:p.Arg1032Trp
XM_011542671.1:c.3094A>T XP_011540973.1:p.Arg1032Trp
XM_011542672.1:c.3094A>T XP_011540974.1:p.Arg1032Trp
XM_011542673.1:c.3094A>T XP_011540975.1:p.Arg1032Trp
XM_011542674.1:c.3094A>T XP_011540976.1:p.Ser1032Cys
XM_011542675.1:c.3094A>T XP_011540977.1:p.Arg1032Trp
XM_011542676.1:c.3016A>T XP_011540978.1:p.Arg1006Trp
XM_011542677.1:c.2956A>T XP_011540979.1:p.Arg986Trp
XM_011542678.1:c.2956A>T XP_011540980.1:p.Arg986Trp
XM_011542679.1:c.3094A>T XP_011540981.1:p.Arg1032Trp
XM_011542680.1:c.2848A>T XP_011540982.1:p.Arg950Trp
XM_011542681.1:c.3094A>T XP_011540983.1:p.Arg1032Trp
XM_011542682.1:c.1408A>T XP_011540984.1:p.Arg470Trp
XM_011542683.1:c.1408A>T XP_011540985.1:p.Arg470Trp
XM_011542685.1:c.1330A>T XP_011540987.1:p.Arg444Trp
XM_011542686.1:c.1330A>T XP_011540988.1:p.Arg444Trp
XM_011542687.1:c.1270A>T XP_011540989.1:p.Arg424Trp
XM_011542688.1:c.1069A>T XP_011540990.1:p.Arg357Trp
XM_017017364.1:c.3094A>T XP_016872853.1:p.Ser1032Cys
XM_017017365.1:c.3094A>T XP_016872854.1:p.Ser1032Cys
XM_017017366.1:c.3094A>T XP_016872855.1:p.Ser1032Cys
XM_017017367.1:c.3094A>T XP_016872856.1:p.Ser1032Cys
XM_017017368.1:c.3094A>T XP_016872857.1:p.Ser1032Cys
XM_017017369.1:c.3094A>T XP_016872858.1:p.Ser1032Cys
XM_017017370.1:c.3094A>T XP_016872859.1:p.Ser1032Cys
XM_017017371.1:c.3016A>T XP_016872860.1:p.Ser1006Cys
XM_017017372.1:c.3016A>T XP_016872861.1:p.Arg1006Trp
XM_017017373.2:c.2956A>T XP_016872862.1:p.Ser986Cys
XM_017017374.1:c.2956A>T XP_016872863.1:p.Ser986Cys
XM_017017375.2:c.2956A>T XP_016872864.1:p.Ser986Cys
XM_017017376.1:c.3094A>T XP_016872865.1:p.Ser1032Cys
XM_017017377.2:c.2848A>T XP_016872866.1:p.Ser950Cys
XM_017017378.1:c.3094A>T XP_016872867.1:p.Ser1032Cys
XM_017017379.1:c.1408A>T XP_016872868.1:p.Ser470Cys
XM_017017380.1:c.1408A>T XP_016872869.1:p.Ser470Cys
XM_017017381.1:c.1330A>T XP_016872870.1:p.Ser444Cys
XM_017017382.1:c.1330A>T XP_016872871.1:p.Ser444Cys
XM_017017383.1:c.1270A>T XP_016872872.1:p.Ser424Cys
XM_017017384.1:c.1270A>T XP_016872873.1:p.Ser424Cys
XM_017017385.1:c.1069A>T XP_016872874.1:p.Ser357Cys
XM_017017386.1:c.1192A>T XP_016872875.1:p.Arg398Trp
XR_001747793.1:n.3512A>T
XR_001747794.1:n.3512A>T
XR_002957132.1:n.3512A>T
XR_002957133.1:n.3512A>T
XR_428971.2:n.3512A>T
XR_428971.3:n.3512A>T
XR_947808.1:n.3512A>T
XR_947809.1:n.3512A>T
XR_947810.1:n.3512A>T
XR_947811.1:n.3512A>T