Canonical Allele Identifier: CA10613412

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19910671A>G , CM000664.2:g.19910671A>G	GRCh38
NC_000002.11:g.20110432A>G , CM000664.1:g.20110432A>G	GRCh37
NC_000002.10:g.19973913A>G	NCBI36
NG_021212.1:g.84453T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.*2887T>C MANE Select	ENSP00000281405.5:n.*2887T>C
ENST00000345530.8:c.*2887T>C MANE Plus Clinical	ENSP00000314444.5:n.*2887T>C
ENST00000281405.8:c.*2887T>C	ENSP00000281405.4:n.*2887T>C
ENST00000345530.7:c.*2887T>C	ENSP00000314444.5:n.*2887T>C
NM_001006657.1:c.*2887T>C	NP_001006658.1:n.*2887T>C
NM_020779.3:c.*2887T>C	NP_065830.2:n.*2887T>C
XM_011533007.1:c.*2887T>C	XP_011531309.1:n.*2887T>C
XM_011533007.2:c.*2887T>C	XP_011531309.1:n.*2887T>C
XR_426989.3:n.6333T>C
NM_001006657.2:c.*2887T>C MANE Plus Clinical	NP_001006658.1:n.*2887T>C
NM_020779.4:c.*2887T>C MANE Select	NP_065830.2:n.*2887T>C