Canonical Allele Identifier: CA372187058

Gene: WASHC5 WASHC5-AS1

Linked Data

• MyVariant Identifiers: chr8:g.126056090C>T (hg19) ; chr8:g.125043848C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125043848C>T , CM000670.2:g.125043848C>T	GRCh38
NC_000008.10:g.126056090C>T , CM000670.1:g.126056090C>T	GRCh37
NC_000008.9:g.126125272C>T	NCBI36
NG_012636.1:g.52972G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.2827G>A (WASHC5) MANE Select	ENSP00000318016.7:p.Ala943Thr
ENST00000318410.11:c.2827G>A (WASHC5)	ENSP00000318016.7:p.Ala943Thr
ENST00000517845.5:c.2383G>A (WASHC5)	ENSP00000429676.1:p.Ala795Thr
NM_014846.3:c.2827G>A (WASHC5)	NP_055661.3:p.Ala943Thr
XM_005251120.2:c.2383G>A (WASHC5)	XP_005251177.1:p.Ala795Thr
XM_011517409.1:c.2827G>A (WASHC5)	XP_011515711.1:p.Ala943Thr
XM_011517410.1:c.2827G>A (WASHC5)	XP_011515712.1:p.Ala943Thr
NM_001330609.1:c.2383G>A (WASHC5)	NP_001317538.1:p.Ala795Thr
XM_017014113.2:c.2827G>A (WASHC5)	XP_016869602.1:p.Ala943Thr
NM_014846.4:c.2827G>A (WASHC5) MANE Select	NP_055661.3:p.Ala943Thr
NM_001330609.2:c.2383G>A (WASHC5)	NP_001317538.1:p.Ala795Thr
NR_170219.1:n.97-651C>T (WASHC5-AS1)