Canonical Allele Identifier: CA2688510075

Gene: WASHC5

Linked Data

• gnomAD v4: 8-125057476-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125057481_125057482del , CM000670.2:g.125057481_125057482del	GRCh38
NC_000008.10:g.126069723_126069724del , CM000670.1:g.126069723_126069724del	GRCh37
NC_000008.9:g.126138905_126138906del	NCBI36
NG_012636.1:g.39342_39343del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.1875+78_1875+79del MANE Select	ENSP00000318016.7:n.1875+78_1875+79del
ENST00000318410.11:c.1875+78_1875+79del	ENSP00000318016.7:n.1875+78_1875+79del
ENST00000517845.5:c.1431+78_1431+79del	ENSP00000429676.1:n.1431+78_1431+79del
NM_014846.3:c.1875+78_1875+79del	NP_055661.3:n.1875+78_1875+79del
XM_005251120.2:c.1431+78_1431+79del	XP_005251177.1:n.1431+78_1431+79del
XM_011517409.1:c.1875+78_1875+79del	XP_011515711.1:n.1875+78_1875+79del
XM_011517410.1:c.1875+78_1875+79del	XP_011515712.1:n.1875+78_1875+79del
NM_001330609.1:c.1431+78_1431+79del	NP_001317538.1:n.1431+78_1431+79del
XM_017014113.2:c.1875+78_1875+79del	XP_016869602.1:n.1875+78_1875+79del
NM_014846.4:c.1875+78_1875+79del MANE Select	NP_055661.3:n.1875+78_1875+79del
NM_001330609.2:c.1431+78_1431+79del	NP_001317538.1:n.1431+78_1431+79del