Canonical Allele Identifier: CA2493001101
Gene: WDR35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19989164_19989168delinsCCTGT , CM000664.2:g.19989164_19989168delinsCCTGT GRCh38
NC_000002.11:g.20188925_20188929delinsCCTGT , CM000664.1:g.20188925_20188929delinsCCTGT GRCh37
NC_000002.10:g.20052406_20052410delinsCCTGT NCBI36
NG_021212.1:g.5956_5960delinsACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000281405.9:c.139_142+1delinsACAGG
ENST00000345530.8:c.139_142+1delinsACAGG
ENST00000281405.8:c.139_142+1delinsACAGG
ENST00000345530.7:c.139_142+1delinsACAGG
ENST00000414212.5:c.139_142+1delinsACAGG
NM_001006657.1:c.139_142+1delinsACAGG
NM_020779.3:c.139_142+1delinsACAGG
XR_426989.2:n.172_175+1delinsACAGG
XR_939699.1:n.172_175+1delinsACAGG
XR_001738862.1:n.172_175+1delinsACAGG
XR_426989.3:n.172_175+1delinsACAGG
XR_939699.3:n.172_175+1delinsACAGG
NM_001006657.2:c.139_142+1delinsACAGG
NM_020779.4:c.139_142+1delinsACAGG