Canonical Allele Identifier: CA1817263215

Gene: WASHC5

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125057476_125057477delinsTG , CM000670.2:g.125057476_125057477delinsTG	GRCh38
NC_000008.10:g.126069718_126069719delinsTG , CM000670.1:g.126069718_126069719delinsTG	GRCh37
NC_000008.9:g.126138900_126138901delinsTG	NCBI36
NG_012636.1:g.39343_39344delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.1875+79_1875+80delinsCA MANE Select	ENSP00000318016.7:n.1875+79_1875+80delinsCA
ENST00000318410.11:c.1875+79_1875+80delinsCA	ENSP00000318016.7:n.1875+79_1875+80delinsCA
ENST00000517845.5:c.1431+79_1431+80delinsCA	ENSP00000429676.1:n.1431+79_1431+80delinsCA
NM_014846.3:c.1875+79_1875+80delinsCA	NP_055661.3:n.1875+79_1875+80delinsCA
XM_005251120.2:c.1431+79_1431+80delinsCA	XP_005251177.1:n.1431+79_1431+80delinsCA
XM_011517409.1:c.1875+79_1875+80delinsCA	XP_011515711.1:n.1875+79_1875+80delinsCA
XM_011517410.1:c.1875+79_1875+80delinsCA	XP_011515712.1:n.1875+79_1875+80delinsCA
NM_001330609.1:c.1431+79_1431+80delinsCA	NP_001317538.1:n.1431+79_1431+80delinsCA
XM_017014113.2:c.1875+79_1875+80delinsCA	XP_016869602.1:n.1875+79_1875+80delinsCA
NM_014846.4:c.1875+79_1875+80delinsCA MANE Select	NP_055661.3:n.1875+79_1875+80delinsCA
NM_001330609.2:c.1431+79_1431+80delinsCA	NP_001317538.1:n.1431+79_1431+80delinsCA