Canonical Allele Identifier: CA372191344
Gene: WASHC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125057608A>C , CM000670.2:g.125057608A>C GRCh38
NC_000008.10:g.126069850A>C , CM000670.1:g.126069850A>C GRCh37
NC_000008.9:g.126139032A>C NCBI36
NG_012636.1:g.39212T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318410.12:c.1823T>G MANE Select ENSP00000318016.7:p.Leu608Arg
ENST00000318410.11:c.1823T>G ENSP00000318016.7:p.Leu608Arg
ENST00000517845.5:c.1379T>G ENSP00000429676.1:p.Leu460Arg
NM_014846.3:c.1823T>G NP_055661.3:p.Leu608Arg
XM_005251120.2:c.1379T>G XP_005251177.1:p.Leu460Arg
XM_011517409.1:c.1823T>G XP_011515711.1:p.Leu608Arg
XM_011517410.1:c.1823T>G XP_011515712.1:p.Leu608Arg
NM_001330609.1:c.1379T>G NP_001317538.1:p.Leu460Arg
XM_017014113.2:c.1823T>G XP_016869602.1:p.Leu608Arg
NM_014846.4:c.1823T>G MANE Select NP_055661.3:p.Leu608Arg
NM_001330609.2:c.1379T>G NP_001317538.1:p.Leu460Arg