Canonical Allele Identifier: CA43398627

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19937734A>G , CM000664.2:g.19937734A>G	GRCh38
NC_000002.11:g.20137495A>G , CM000664.1:g.20137495A>G	GRCh37
NC_000002.10:g.20000976A>G	NCBI36
NG_021212.1:g.57390T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2267+9T>C MANE Select	NP_065830.2:n.2267+9T>C
ENST00000281405.9:c.2267+9T>C MANE Select	ENSP00000281405.5:n.2267+9T>C
NM_001006657.2:c.2300+9T>C MANE Plus Clinical	NP_001006658.1:n.2300+9T>C
ENST00000345530.8:c.2300+9T>C MANE Plus Clinical	ENSP00000314444.5:n.2300+9T>C
NM_001006657.1:c.2300+9T>C	NP_001006658.1:n.2300+9T>C
NM_020779.3:c.2267+9T>C	NP_065830.2:n.2267+9T>C
ENST00000281405.8:c.2267+9T>C	ENSP00000281405.4:n.2267+9T>C
ENST00000345530.7:c.2300+9T>C	ENSP00000314444.5:n.2300+9T>C
ENST00000414212.5:c.2300+9T>C	ENSP00000390802.1:n.2300+9T>C
ENST00000445063.5:c.1743+9T>C
ENST00000453014.1:c.905+9T>C	ENSP00000404409.1:n.905+9T>C
XM_011533007.1:c.995+9T>C	XP_011531309.1:n.995+9T>C
XM_011533007.2:c.995+9T>C	XP_011531309.1:n.995+9T>C
XR_001738862.1:n.2244+9T>C
XR_426989.2:n.2300+9T>C
XR_426989.3:n.2300+9T>C