Canonical Allele Identifier: CA372191233

Gene: WASHC5

Linked Data

• MyVariant Identifiers: chr8:g.126069798T>G (hg19) ; chr8:g.125057556T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125057556T>G , CM000670.2:g.125057556T>G	GRCh38
NC_000008.10:g.126069798T>G , CM000670.1:g.126069798T>G	GRCh37
NC_000008.9:g.126138980T>G	NCBI36
NG_012636.1:g.39264A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318410.12:c.1875A>C MANE Select	ENSP00000318016.7:p.Lys625Asn
ENST00000318410.11:c.1875A>C	ENSP00000318016.7:p.Lys625Asn
ENST00000517845.5:c.1431A>C	ENSP00000429676.1:p.Lys477Asn
NM_014846.3:c.1875A>C	NP_055661.3:p.Lys625Asn
XM_005251120.2:c.1431A>C	XP_005251177.1:p.Lys477Asn
XM_011517409.1:c.1875A>C	XP_011515711.1:p.Lys625Asn
XM_011517410.1:c.1875A>C	XP_011515712.1:p.Lys625Asn
NM_001330609.1:c.1431A>C	NP_001317538.1:p.Lys477Asn
XM_017014113.2:c.1875A>C	XP_016869602.1:p.Lys625Asn
NM_014846.4:c.1875A>C MANE Select	NP_055661.3:p.Lys625Asn
NM_001330609.2:c.1431A>C	NP_001317538.1:p.Lys477Asn