Canonical Allele Identifier: CA4873263
Community Standard Title: NM_014846.4(WASHC5):c.3276C>T (p.Thr1092=)
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125032300G>A , CM000670.2:g.125032300G>A GRCh38
NC_000008.10:g.126044542G>A , CM000670.1:g.126044542G>A GRCh37
NC_000008.9:g.126113724G>A NCBI36
NG_012636.1:g.64520C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014846.4:c.3276C>T MANE Select NP_055661.3:p.Thr1092=
ENST00000318410.12:c.3276C>T MANE Select ENSP00000318016.7:p.Thr1092=
NM_001330609.1:c.2832C>T NP_001317538.1:p.Thr944=
NM_001330609.2:c.2832C>T NP_001317538.1:p.Thr944=
NM_014846.3:c.3276C>T NP_055661.3:p.Thr1092=
ENST00000318410.11:c.3276C>T ENSP00000318016.7:p.Thr1092=
ENST00000517845.5:c.2832C>T ENSP00000429676.1:p.Thr944=
ENST00000519042.2:n.415C>T
XM_005251120.2:c.2832C>T XP_005251177.1:p.Thr944=
XM_017014113.2:c.3276C>T XP_016869602.1:p.Thr1092=