Canonical Allele Identifier: CA2493001094

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989142_19989144delinsCAT , CM000664.2:g.19989142_19989144delinsCAT	GRCh38
NC_000002.11:g.20188903_20188905delinsCAT , CM000664.1:g.20188903_20188905delinsCAT	GRCh37
NC_000002.10:g.20052384_20052386delinsCAT	NCBI36
NG_021212.1:g.5980_5982delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.142+21_142+23delinsATG MANE Select	ENSP00000281405.5:n.142+21_142+23delinsATG
ENST00000345530.8:c.142+21_142+23delinsATG MANE Plus Clinical	ENSP00000314444.5:n.142+21_142+23delinsATG
ENST00000281405.8:c.142+21_142+23delinsATG	ENSP00000281405.4:n.142+21_142+23delinsATG
ENST00000345530.7:c.142+21_142+23delinsATG	ENSP00000314444.5:n.142+21_142+23delinsATG
ENST00000414212.5:c.142+21_142+23delinsATG	ENSP00000390802.1:n.142+21_142+23delinsATG
NM_001006657.1:c.142+21_142+23delinsATG	NP_001006658.1:n.142+21_142+23delinsATG
NM_020779.3:c.142+21_142+23delinsATG	NP_065830.2:n.142+21_142+23delinsATG
XR_426989.2:n.175+21_175+23delinsATG
XR_939699.1:n.175+21_175+23delinsATG
XR_001738862.1:n.175+21_175+23delinsATG
XR_426989.3:n.175+21_175+23delinsATG
XR_939699.3:n.175+21_175+23delinsATG
NM_001006657.2:c.142+21_142+23delinsATG MANE Plus Clinical	NP_001006658.1:n.142+21_142+23delinsATG
NM_020779.4:c.142+21_142+23delinsATG MANE Select	NP_065830.2:n.142+21_142+23delinsATG