Canonical Allele Identifier: CA372181094

Gene: WASHC5

Linked Data

• MyVariant Identifiers: chr8:g.126044501G>C (hg19) ; chr8:g.125032259G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125032259G>C , CM000670.2:g.125032259G>C	GRCh38
NC_000008.10:g.126044501G>C , CM000670.1:g.126044501G>C	GRCh37
NC_000008.9:g.126113683G>C	NCBI36
NG_012636.1:g.64561C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.3317C>G MANE Select	ENSP00000318016.7:p.Thr1106Arg
ENST00000318410.11:c.3317C>G	ENSP00000318016.7:p.Thr1106Arg
ENST00000517845.5:c.2873C>G	ENSP00000429676.1:p.Thr958Arg
ENST00000519042.2:n.456C>G
NM_014846.3:c.3317C>G	NP_055661.3:p.Thr1106Arg
XM_005251120.2:c.2873C>G	XP_005251177.1:p.Thr958Arg
NM_001330609.1:c.2873C>G	NP_001317538.1:p.Thr958Arg
XM_017014113.2:c.3317C>G	XP_016869602.1:p.Thr1106Arg
NM_014846.4:c.3317C>G MANE Select	NP_055661.3:p.Thr1106Arg
NM_001330609.2:c.2873C>G	NP_001317538.1:p.Thr958Arg