Canonical Allele Identifier: CA1817262541
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125056817C= , CM000670.2:g.125056817C= GRCh38
NC_000008.10:g.126069059C= , CM000670.1:g.126069059C= GRCh37
NC_000008.9:g.126138241C= NCBI36
NG_012636.1:g.40003G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1876G= MANE Select ENSP00000318016.7:p.Val626=
ENST00000318410.11:c.1876G= ENSP00000318016.7:p.Val626=
ENST00000517845.5:c.1432G= ENSP00000429676.1:p.Val478=
NM_014846.3:c.1876G= NP_055661.3:p.Val626=
XM_005251120.2:c.1432G= XP_005251177.1:p.Val478=
XM_011517409.1:c.1876G= XP_011515711.1:p.Val626=
XM_011517410.1:c.1876G= XP_011515712.1:p.Val626=
NM_001330609.1:c.1432G= NP_001317538.1:p.Val478=
XM_017014113.2:c.1876G= XP_016869602.1:p.Val626=
NM_014846.4:c.1876G= MANE Select NP_055661.3:p.Val626=
NM_001330609.2:c.1432G= NP_001317538.1:p.Val478=