Canonical Allele Identifier: CA345948449

Gene: WDR35

Linked Data

• MyVariant Identifiers: chr2:g.20188929T>A (hg19) ; chr2:g.19989168T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989168T>A , CM000664.2:g.19989168T>A	GRCh38
NC_000002.11:g.20188929T>A , CM000664.1:g.20188929T>A	GRCh37
NC_000002.10:g.20052410T>A	NCBI36
NG_021212.1:g.5956A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.139A>T MANE Select	ENSP00000281405.5:p.Thr47Ser
ENST00000345530.8:c.139A>T MANE Plus Clinical	ENSP00000314444.5:p.Thr47Ser
ENST00000281405.8:c.139A>T	ENSP00000281405.4:p.Thr47Ser
ENST00000345530.7:c.139A>T	ENSP00000314444.5:p.Thr47Ser
ENST00000414212.5:c.139A>T	ENSP00000390802.1:p.Thr47Ser
NM_001006657.1:c.139A>T	NP_001006658.1:p.Thr47Ser
NM_020779.3:c.139A>T	NP_065830.2:p.Thr47Ser
XR_426989.2:n.172A>T
XR_939699.1:n.172A>T
XR_001738862.1:n.172A>T
XR_426989.3:n.172A>T
XR_939699.3:n.172A>T
NM_001006657.2:c.139A>T MANE Plus Clinical	NP_001006658.1:p.Thr47Ser
NM_020779.4:c.139A>T MANE Select	NP_065830.2:p.Thr47Ser