Canonical Allele Identifier: CA1817263306
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125057547_125057548delinsAT , CM000670.2:g.125057547_125057548delinsAT GRCh38
NC_000008.10:g.126069789_126069790delinsAT , CM000670.1:g.126069789_126069790delinsAT GRCh37
NC_000008.9:g.126138971_126138972delinsAT NCBI36
NG_012636.1:g.39272_39273delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1875+8_1875+9delinsAT MANE Select ENSP00000318016.7:n.1875+8_1875+9delinsAT
ENST00000318410.11:c.1875+8_1875+9delinsAT ENSP00000318016.7:n.1875+8_1875+9delinsAT
ENST00000517845.5:c.1431+8_1431+9delinsAT ENSP00000429676.1:n.1431+8_1431+9delinsAT
NM_014846.3:c.1875+8_1875+9delinsAT NP_055661.3:n.1875+8_1875+9delinsAT
XM_005251120.2:c.1431+8_1431+9delinsAT XP_005251177.1:n.1431+8_1431+9delinsAT
XM_011517409.1:c.1875+8_1875+9delinsAT XP_011515711.1:n.1875+8_1875+9delinsAT
XM_011517410.1:c.1875+8_1875+9delinsAT XP_011515712.1:n.1875+8_1875+9delinsAT
NM_001330609.1:c.1431+8_1431+9delinsAT NP_001317538.1:n.1431+8_1431+9delinsAT
XM_017014113.2:c.1875+8_1875+9delinsAT XP_016869602.1:n.1875+8_1875+9delinsAT
NM_014846.4:c.1875+8_1875+9delinsAT MANE Select NP_055661.3:n.1875+8_1875+9delinsAT
NM_001330609.2:c.1431+8_1431+9delinsAT NP_001317538.1:n.1431+8_1431+9delinsAT