Canonical Allele Identifier: CA2688510103

Gene: WASHC5

Linked Data

• gnomAD v4: 8-125057516-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125057516T>A , CM000670.2:g.125057516T>A	GRCh38
NC_000008.10:g.126069758T>A , CM000670.1:g.126069758T>A	GRCh37
NC_000008.9:g.126138940T>A	NCBI36
NG_012636.1:g.39304A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318410.12:c.1875+40A>T MANE Select	ENSP00000318016.7:n.1875+40A>T
ENST00000318410.11:c.1875+40A>T	ENSP00000318016.7:n.1875+40A>T
ENST00000517845.5:c.1431+40A>T	ENSP00000429676.1:n.1431+40A>T
NM_014846.3:c.1875+40A>T	NP_055661.3:n.1875+40A>T
XM_005251120.2:c.1431+40A>T	XP_005251177.1:n.1431+40A>T
XM_011517409.1:c.1875+40A>T	XP_011515711.1:n.1875+40A>T
XM_011517410.1:c.1875+40A>T	XP_011515712.1:n.1875+40A>T
NM_001330609.1:c.1431+40A>T	NP_001317538.1:n.1431+40A>T
XM_017014113.2:c.1875+40A>T	XP_016869602.1:n.1875+40A>T
NM_014846.4:c.1875+40A>T MANE Select	NP_055661.3:n.1875+40A>T
NM_001330609.2:c.1431+40A>T	NP_001317538.1:n.1431+40A>T