Canonical Allele Identifier: CA1817263231

Gene: WASHC5

Linked Data

• dbSNP Id: rs1816443907
• gnomAD v4: 8-125057490-A-T

Genomic Alleles

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

Transcript Alleles

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