Canonical Allele Identifier: CA1817263222
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125057487A= , CM000670.2:g.125057487A= GRCh38
NC_000008.10:g.126069729A= , CM000670.1:g.126069729A= GRCh37
NC_000008.9:g.126138911A= NCBI36
NG_012636.1:g.39333T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1875+69T= MANE Select ENSP00000318016.7:n.1875+69T=
ENST00000318410.11:c.1875+69T= ENSP00000318016.7:n.1875+69T=
ENST00000517845.5:c.1431+69T= ENSP00000429676.1:n.1431+69T=
NM_014846.3:c.1875+69T= NP_055661.3:n.1875+69T=
XM_005251120.2:c.1431+69T= XP_005251177.1:n.1431+69T=
XM_011517409.1:c.1875+69T= XP_011515711.1:n.1875+69T=
XM_011517410.1:c.1875+69T= XP_011515712.1:n.1875+69T=
NM_001330609.1:c.1431+69T= NP_001317538.1:n.1431+69T=
XM_017014113.2:c.1875+69T= XP_016869602.1:n.1875+69T=
NM_014846.4:c.1875+69T= MANE Select NP_055661.3:n.1875+69T=
NM_001330609.2:c.1431+69T= NP_001317538.1:n.1431+69T=