Canonical Allele Identifier: CA1817266728
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125061192T= , CM000670.2:g.125061192T= GRCh38
NC_000008.10:g.126073434T= , CM000670.1:g.126073434T= GRCh37
NC_000008.9:g.126142616T= NCBI36
NG_012636.1:g.35628A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1411A= MANE Select ENSP00000318016.7:p.Asn471=
ENST00000318410.11:c.1411A= ENSP00000318016.7:p.Asn471=
ENST00000517845.5:c.967A= ENSP00000429676.1:p.Asn323=
NM_014846.3:c.1411A= NP_055661.3:p.Asn471=
XM_005251120.2:c.967A= XP_005251177.1:p.Asn323=
XM_011517409.1:c.1411A= XP_011515711.1:p.Asn471=
XM_011517410.1:c.1411A= XP_011515712.1:p.Asn471=
NM_001330609.1:c.967A= NP_001317538.1:p.Asn323=
XM_017014113.2:c.1411A= XP_016869602.1:p.Asn471=
NM_014846.4:c.1411A= MANE Select NP_055661.3:p.Asn471=
NM_001330609.2:c.967A= NP_001317538.1:p.Asn323=