Canonical Allele Identifier: CA372181919

Gene: WASHC5

Linked Data

• MyVariant Identifiers: chr8:g.126044588A>C (hg19) ; chr8:g.125032346A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125032346A>C , CM000670.2:g.125032346A>C	GRCh38
NC_000008.10:g.126044588A>C , CM000670.1:g.126044588A>C	GRCh37
NC_000008.9:g.126113770A>C	NCBI36
NG_012636.1:g.64474T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.3230T>G MANE Select	ENSP00000318016.7:p.Val1077Gly
ENST00000318410.11:c.3230T>G	ENSP00000318016.7:p.Val1077Gly
ENST00000517845.5:c.2786T>G	ENSP00000429676.1:p.Val929Gly
ENST00000519042.2:n.369T>G
NM_014846.3:c.3230T>G	NP_055661.3:p.Val1077Gly
XM_005251120.2:c.2786T>G	XP_005251177.1:p.Val929Gly
NM_001330609.1:c.2786T>G	NP_001317538.1:p.Val929Gly
XM_017014113.2:c.3230T>G	XP_016869602.1:p.Val1077Gly
NM_014846.4:c.3230T>G MANE Select	NP_055661.3:p.Val1077Gly
NM_001330609.2:c.2786T>G	NP_001317538.1:p.Val929Gly