Canonical Allele Identifier: CA1817263497
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125057686T= , CM000670.2:g.125057686T= GRCh38
NC_000008.10:g.126069928T= , CM000670.1:g.126069928T= GRCh37
NC_000008.9:g.126139110T= NCBI36
NG_012636.1:g.39134A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1765-20A= MANE Select ENSP00000318016.7:n.1765-20A=
ENST00000318410.11:c.1765-20A= ENSP00000318016.7:n.1765-20A=
ENST00000517845.5:c.1321-20A= ENSP00000429676.1:n.1321-20A=
NM_014846.3:c.1765-20A= NP_055661.3:n.1765-20A=
XM_005251120.2:c.1321-20A= XP_005251177.1:n.1321-20A=
XM_011517409.1:c.1765-20A= XP_011515711.1:n.1765-20A=
XM_011517410.1:c.1765-20A= XP_011515712.1:n.1765-20A=
NM_001330609.1:c.1321-20A= NP_001317538.1:n.1321-20A=
XM_017014113.2:c.1765-20A= XP_016869602.1:n.1765-20A=
NM_014846.4:c.1765-20A= MANE Select NP_055661.3:n.1765-20A=
NM_001330609.2:c.1321-20A= NP_001317538.1:n.1321-20A=