Canonical Allele Identifier: CA345942376

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19932405C>A , CM000664.2:g.19932405C>A	GRCh38
NC_000002.11:g.20132166C>A , CM000664.1:g.20132166C>A	GRCh37
NC_000002.10:g.19995647C>A	NCBI36
NG_021212.1:g.62719G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2701G>T MANE Select	NP_065830.2:p.Glu901Ter
ENST00000281405.9:c.2701G>T MANE Select	ENSP00000281405.5:p.Glu901Ter
NM_001006657.2:c.2734G>T MANE Plus Clinical	NP_001006658.1:p.Glu912Ter
ENST00000345530.8:c.2734G>T MANE Plus Clinical	ENSP00000314444.5:p.Glu912Ter
NM_001006657.1:c.2734G>T	NP_001006658.1:p.Glu912Ter
NM_020779.3:c.2701G>T	NP_065830.2:p.Glu901Ter
ENST00000281405.8:c.2701G>T	ENSP00000281405.4:p.Glu901Ter
ENST00000345530.7:c.2734G>T	ENSP00000314444.5:p.Glu912Ter
ENST00000414212.5:c.*116G>T	ENSP00000390802.1:n.*116G>T
ENST00000445063.5:c.2024-996G>T
XM_011533007.1:c.1429G>T	XP_011531309.1:p.Glu477Ter
XM_011533007.2:c.1429G>T	XP_011531309.1:p.Glu477Ter
XR_001738862.1:n.2678G>T
XR_426989.2:n.2734G>T
XR_426989.3:n.2734G>T