Canonical Allele Identifier: CA462766871

Gene: WASHC5

Linked Data

• MyVariant Identifiers: chr8:g.126044512A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125032270A>G , CM000670.2:g.125032270A>G	GRCh38
NC_000008.10:g.126044512A>G , CM000670.1:g.126044512A>G	GRCh37
NC_000008.9:g.126113694A>G	NCBI36
NG_012636.1:g.64550T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.3306T>C MANE Select	ENSP00000318016.7:p.Phe1102=
ENST00000318410.11:c.3306T>C	ENSP00000318016.7:p.Phe1102=
ENST00000517845.5:c.2862T>C	ENSP00000429676.1:p.Phe954=
ENST00000519042.2:n.445T>C
NM_014846.3:c.3306T>C	NP_055661.3:p.Phe1102=
XM_005251120.2:c.2862T>C	XP_005251177.1:p.Phe954=
NM_001330609.1:c.2862T>C	NP_001317538.1:p.Phe954=
XM_017014113.2:c.3306T>C	XP_016869602.1:p.Phe1102=
NM_014846.4:c.3306T>C MANE Select	NP_055661.3:p.Phe1102=
NM_001330609.2:c.2862T>C	NP_001317538.1:p.Phe954=