Canonical Allele Identifier: CA1817239135
Community Standard Title: NM_014846.4(WASHC5):c.2888A= (p.Asn963=)
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125039861T= , CM000670.2:g.125039861T= GRCh38
NC_000008.10:g.126052103T= , CM000670.1:g.126052103T= GRCh37
NC_000008.9:g.126121285T= NCBI36
NG_012636.1:g.56959A=

Transcript Alleles

HGVS Amino-acid Change
NM_014846.4:c.2888A= MANE Select NP_055661.3:p.Asn963=
ENST00000318410.12:c.2888A= MANE Select ENSP00000318016.7:p.Asn963=
NM_001330609.1:c.2444A= NP_001317538.1:p.Asn815=
NM_001330609.2:c.2444A= NP_001317538.1:p.Asn815=
NM_014846.3:c.2888A= NP_055661.3:p.Asn963=
ENST00000318410.11:c.2888A= ENSP00000318016.7:p.Asn963=
ENST00000517845.5:c.2444A= ENSP00000429676.1:p.Asn815=
XM_005251120.2:c.2444A= XP_005251177.1:p.Asn815=
XM_011517409.1:c.2888A= XP_011515711.1:p.Asn963=
XM_011517410.1:c.2888A= XP_011515712.1:p.Asn963=
XM_017014113.2:c.2888A= XP_016869602.1:p.Asn963=