Canonical Allele Identifier: CA345945775

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19960553C>G , CM000664.2:g.19960553C>G	GRCh38
NC_000002.11:g.20160314C>G , CM000664.1:g.20160314C>G	GRCh37
NC_000002.10:g.20023795C>G	NCBI36
NG_021212.1:g.34571G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.1255+1G>C MANE Select	NP_065830.2:n.1255+1G>C
ENST00000281405.9:c.1255+1G>C MANE Select	ENSP00000281405.5:n.1255+1G>C
NM_001006657.2:c.1288+1G>C MANE Plus Clinical	NP_001006658.1:n.1288+1G>C
ENST00000345530.8:c.1288+1G>C MANE Plus Clinical	ENSP00000314444.5:n.1288+1G>C
NM_001006657.1:c.1288+1G>C	NP_001006658.1:n.1288+1G>C
NM_020779.3:c.1255+1G>C	NP_065830.2:n.1255+1G>C
ENST00000281405.8:c.1255+1G>C	ENSP00000281405.4:n.1255+1G>C
ENST00000345530.7:c.1288+1G>C	ENSP00000314444.5:n.1288+1G>C
ENST00000414212.5:c.1288+1G>C	ENSP00000390802.1:n.1288+1G>C
ENST00000445063.5:c.731+6171G>C
XM_011533007.1:c.-18+6171G>C	XP_011531309.1:n.-18+6171G>C
XM_011533007.2:c.-18+6171G>C	XP_011531309.1:n.-18+6171G>C
XR_001738862.1:n.1288+1G>C
XR_426989.2:n.1288+1G>C
XR_426989.3:n.1288+1G>C
XR_939699.1:n.1288+1G>C
XR_939699.3:n.1288+1G>C