Canonical Allele Identifier: CA372181316

Gene: WASHC5

Linked Data

• MyVariant Identifiers: chr8:g.126044522A>T (hg19) ; chr8:g.125032280A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125032280A>T , CM000670.2:g.125032280A>T	GRCh38
NC_000008.10:g.126044522A>T , CM000670.1:g.126044522A>T	GRCh37
NC_000008.9:g.126113704A>T	NCBI36
NG_012636.1:g.64540T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.3296T>A MANE Select	ENSP00000318016.7:p.Ile1099Asn
ENST00000318410.11:c.3296T>A	ENSP00000318016.7:p.Ile1099Asn
ENST00000517845.5:c.2852T>A	ENSP00000429676.1:p.Ile951Asn
ENST00000519042.2:n.435T>A
NM_014846.3:c.3296T>A	NP_055661.3:p.Ile1099Asn
XM_005251120.2:c.2852T>A	XP_005251177.1:p.Ile951Asn
NM_001330609.1:c.2852T>A	NP_001317538.1:p.Ile951Asn
XM_017014113.2:c.3296T>A	XP_016869602.1:p.Ile1099Asn
NM_014846.4:c.3296T>A MANE Select	NP_055661.3:p.Ile1099Asn
NM_001330609.2:c.2852T>A	NP_001317538.1:p.Ile951Asn