Canonical Allele Identifier: CA2688510087

Gene: WASHC5

Linked Data

• gnomAD v4: 8-125057490-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125057490A>G , CM000670.2:g.125057490A>G	GRCh38
NC_000008.10:g.126069732A>G , CM000670.1:g.126069732A>G	GRCh37
NC_000008.9:g.126138914A>G	NCBI36
NG_012636.1:g.39330T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318410.12:c.1875+66T>C MANE Select	ENSP00000318016.7:n.1875+66T>C
ENST00000318410.11:c.1875+66T>C	ENSP00000318016.7:n.1875+66T>C
ENST00000517845.5:c.1431+66T>C	ENSP00000429676.1:n.1431+66T>C
NM_014846.3:c.1875+66T>C	NP_055661.3:n.1875+66T>C
XM_005251120.2:c.1431+66T>C	XP_005251177.1:n.1431+66T>C
XM_011517409.1:c.1875+66T>C	XP_011515711.1:n.1875+66T>C
XM_011517410.1:c.1875+66T>C	XP_011515712.1:n.1875+66T>C
NM_001330609.1:c.1431+66T>C	NP_001317538.1:n.1431+66T>C
XM_017014113.2:c.1875+66T>C	XP_016869602.1:n.1875+66T>C
NM_014846.4:c.1875+66T>C MANE Select	NP_055661.3:n.1875+66T>C
NM_001330609.2:c.1431+66T>C	NP_001317538.1:n.1431+66T>C