Canonical Allele Identifier: CA1118838014
Gene: WASHC5 HGNC NCBI
WASHC5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1815968533

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125043850_125043852del , CM000670.2:g.125043850_125043852del GRCh38
NC_000008.10:g.126056092_126056094del , CM000670.1:g.126056092_126056094del GRCh37
NC_000008.9:g.126125274_126125276del NCBI36
NG_012636.1:g.52968_52970del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.2823_2825del (WASHC5) MANE Select ENSP00000318016.7:p.Trp941_Thr942delinsCys
ENST00000318410.11:c.2823_2825del (WASHC5) ENSP00000318016.7:p.Trp941_Thr942delinsCys
ENST00000517845.5:c.2379_2381del (WASHC5) ENSP00000429676.1:p.Trp793_Thr794delinsCys
NM_014846.3:c.2823_2825del (WASHC5) NP_055661.3:p.Trp941_Thr942delinsCys
XM_005251120.2:c.2379_2381del (WASHC5) XP_005251177.1:p.Trp793_Thr794delinsCys
XM_011517409.1:c.2823_2825del (WASHC5) XP_011515711.1:p.Trp941_Thr942delinsCys
XM_011517410.1:c.2823_2825del (WASHC5) XP_011515712.1:p.Trp941_Thr942delinsCys
NM_001330609.1:c.2379_2381del (WASHC5) NP_001317538.1:p.Trp793_Thr794delinsCys
XM_017014113.2:c.2823_2825del (WASHC5) XP_016869602.1:p.Trp941_Thr942delinsCys
NM_014846.4:c.2823_2825del (WASHC5) MANE Select NP_055661.3:p.Trp941_Thr942delinsCys
NM_001330609.2:c.2379_2381del (WASHC5) NP_001317538.1:p.Trp793_Thr794delinsCys
NR_170219.1:n.97-649_97-647del (WASHC5-AS1)