Canonical Allele Identifier: CA4874223

Gene: WASHC5

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125083873T>C , CM000670.2:g.125083873T>C	GRCh38
NC_000008.10:g.126096115T>C , CM000670.1:g.126096115T>C	GRCh37
NC_000008.9:g.126165297T>C	NCBI36
NG_012636.1:g.12947A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014846.4:c.26A>G MANE Select	NP_055661.3:p.Asn9Ser
ENST00000318410.12:c.26A>G MANE Select	ENSP00000318016.7:p.Asn9Ser
NM_001330609.1:c.-258-615A>G	NP_001317538.1:n.-258-615A>G
NM_001330609.2:c.-258-615A>G	NP_001317538.1:n.-258-615A>G
NM_014846.3:c.26A>G	NP_055661.3:p.Asn9Ser
ENST00000318410.11:c.26A>G	ENSP00000318016.7:p.Asn9Ser
ENST00000517845.5:c.-112-1406A>G	ENSP00000429676.1:n.-112-1406A>G
ENST00000519340.5:n.206-97A>G
ENST00000521109.1:n.326A>G
ENST00000523297.5:c.-258-615A>G	ENSP00000427946.1:n.-258-615A>G
XM_005251120.2:c.-258-615A>G	XP_005251177.1:n.-258-615A>G
XM_011517409.1:c.26A>G	XP_011515711.1:p.Asn9Ser
XM_011517410.1:c.26A>G	XP_011515712.1:p.Asn9Ser
XM_017014113.2:c.26A>G	XP_016869602.1:p.Asn9Ser