Canonical Allele Identifier: CA345948528
Gene: WDR35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19989203T>G , CM000664.2:g.19989203T>G GRCh38
NC_000002.11:g.20188964T>G , CM000664.1:g.20188964T>G GRCh37
NC_000002.10:g.20052445T>G NCBI36
NG_021212.1:g.5921A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281405.9:c.104A>C MANE Select ENSP00000281405.5:p.Asp35Ala
ENST00000345530.8:c.104A>C MANE Plus Clinical ENSP00000314444.5:p.Asp35Ala
ENST00000281405.8:c.104A>C ENSP00000281405.4:p.Asp35Ala
ENST00000345530.7:c.104A>C ENSP00000314444.5:p.Asp35Ala
ENST00000414212.5:c.104A>C ENSP00000390802.1:p.Asp35Ala
NM_001006657.1:c.104A>C NP_001006658.1:p.Asp35Ala
NM_020779.3:c.104A>C NP_065830.2:p.Asp35Ala
XR_426989.2:n.137A>C
XR_939699.1:n.137A>C
XR_001738862.1:n.137A>C
XR_426989.3:n.137A>C
XR_939699.3:n.137A>C
NM_001006657.2:c.104A>C MANE Plus Clinical NP_001006658.1:p.Asp35Ala
NM_020779.4:c.104A>C MANE Select NP_065830.2:p.Asp35Ala