Canonical Allele Identifier: CA4873890
Community Standard Title: NM_014846.4(WASHC5):c.1217A>G (p.Asn406Ser)
Gene: WASHC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125067653T>C , CM000670.2:g.125067653T>C GRCh38
NC_000008.10:g.126079895T>C , CM000670.1:g.126079895T>C GRCh37
NC_000008.9:g.126149077T>C NCBI36
NG_012636.1:g.29167A>G

Transcript Alleles

HGVS Amino-acid Change
NM_014846.4:c.1217A>G MANE Select NP_055661.3:p.Asn406Ser
ENST00000318410.12:c.1217A>G MANE Select ENSP00000318016.7:p.Asn406Ser
NM_001330609.1:c.773A>G NP_001317538.1:p.Asn258Ser
NM_001330609.2:c.773A>G NP_001317538.1:p.Asn258Ser
NM_014846.3:c.1217A>G NP_055661.3:p.Asn406Ser
ENST00000318410.11:c.1217A>G ENSP00000318016.7:p.Asn406Ser
ENST00000517845.5:c.773A>G ENSP00000429676.1:p.Asn258Ser
XM_005251120.2:c.773A>G XP_005251177.1:p.Asn258Ser
XM_011517409.1:c.1217A>G XP_011515711.1:p.Asn406Ser
XM_011517410.1:c.1217A>G XP_011515712.1:p.Asn406Ser
XM_017014113.2:c.1217A>G XP_016869602.1:p.Asn406Ser