Canonical Allele Identifier: CA2579247161
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125057462_125057478del , CM000670.2:g.125057462_125057478del GRCh38
NC_000008.10:g.126069704_126069720del , CM000670.1:g.126069704_126069720del GRCh37
NC_000008.9:g.126138886_126138902del NCBI36
NG_012636.1:g.39342_39358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1875+78_1875+94del MANE Select ENSP00000318016.7:n.1875+78_1875+94del
ENST00000318410.11:c.1875+78_1875+94del ENSP00000318016.7:n.1875+78_1875+94del
ENST00000517845.5:c.1431+78_1431+94del ENSP00000429676.1:n.1431+78_1431+94del
NM_014846.3:c.1875+78_1875+94del NP_055661.3:n.1875+78_1875+94del
XM_005251120.2:c.1431+78_1431+94del XP_005251177.1:n.1431+78_1431+94del
XM_011517409.1:c.1875+78_1875+94del XP_011515711.1:n.1875+78_1875+94del
XM_011517410.1:c.1875+78_1875+94del XP_011515712.1:n.1875+78_1875+94del
NM_001330609.1:c.1431+78_1431+94del NP_001317538.1:n.1431+78_1431+94del
XM_017014113.2:c.1875+78_1875+94del XP_016869602.1:n.1875+78_1875+94del
NM_014846.4:c.1875+78_1875+94del MANE Select NP_055661.3:n.1875+78_1875+94del
NM_001330609.2:c.1431+78_1431+94del NP_001317538.1:n.1431+78_1431+94del