Canonical Allele Identifier: CA462767070
Gene: WASHC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.126044569C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125032327C>A , CM000670.2:g.125032327C>A GRCh38
NC_000008.10:g.126044569C>A , CM000670.1:g.126044569C>A GRCh37
NC_000008.9:g.126113751C>A NCBI36
NG_012636.1:g.64493G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.3249G>T MANE Select ENSP00000318016.7:p.Leu1083=
ENST00000318410.11:c.3249G>T ENSP00000318016.7:p.Leu1083=
ENST00000517845.5:c.2805G>T ENSP00000429676.1:p.Leu935=
ENST00000519042.2:n.388G>T
NM_014846.3:c.3249G>T NP_055661.3:p.Leu1083=
XM_005251120.2:c.2805G>T XP_005251177.1:p.Leu935=
NM_001330609.1:c.2805G>T NP_001317538.1:p.Leu935=
XM_017014113.2:c.3249G>T XP_016869602.1:p.Leu1083=
NM_014846.4:c.3249G>T MANE Select NP_055661.3:p.Leu1083=
NM_001330609.2:c.2805G>T NP_001317538.1:p.Leu935=