Canonical Allele Identifier: CA372181282

Gene: WASHC5

Linked Data

• MyVariant Identifiers: chr8:g.126044519C>T (hg19) ; chr8:g.125032277C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125032277C>T , CM000670.2:g.125032277C>T	GRCh38
NC_000008.10:g.126044519C>T , CM000670.1:g.126044519C>T	GRCh37
NC_000008.9:g.126113701C>T	NCBI36
NG_012636.1:g.64543G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.3299G>A MANE Select	ENSP00000318016.7:p.Gly1100Asp
ENST00000318410.11:c.3299G>A	ENSP00000318016.7:p.Gly1100Asp
ENST00000517845.5:c.2855G>A	ENSP00000429676.1:p.Gly952Asp
ENST00000519042.2:n.438G>A
NM_014846.3:c.3299G>A	NP_055661.3:p.Gly1100Asp
XM_005251120.2:c.2855G>A	XP_005251177.1:p.Gly952Asp
NM_001330609.1:c.2855G>A	NP_001317538.1:p.Gly952Asp
XM_017014113.2:c.3299G>A	XP_016869602.1:p.Gly1100Asp
NM_014846.4:c.3299G>A MANE Select	NP_055661.3:p.Gly1100Asp
NM_001330609.2:c.2855G>A	NP_001317538.1:p.Gly952Asp