Canonical Allele Identifier: CA345948537

Gene: WDR35

Linked Data

• MyVariant Identifiers: chr2:g.20188968C>A (hg19) ; chr2:g.19989207C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989207C>A , CM000664.2:g.19989207C>A	GRCh38
NC_000002.11:g.20188968C>A , CM000664.1:g.20188968C>A	GRCh37
NC_000002.10:g.20052449C>A	NCBI36
NG_021212.1:g.5917G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.100G>T MANE Select	ENSP00000281405.5:p.Glu34Ter
ENST00000345530.8:c.100G>T MANE Plus Clinical	ENSP00000314444.5:p.Glu34Ter
ENST00000281405.8:c.100G>T	ENSP00000281405.4:p.Glu34Ter
ENST00000345530.7:c.100G>T	ENSP00000314444.5:p.Glu34Ter
ENST00000414212.5:c.100G>T	ENSP00000390802.1:p.Glu34Ter
NM_001006657.1:c.100G>T	NP_001006658.1:p.Glu34Ter
NM_020779.3:c.100G>T	NP_065830.2:p.Glu34Ter
XR_426989.2:n.133G>T
XR_939699.1:n.133G>T
XR_001738862.1:n.133G>T
XR_426989.3:n.133G>T
XR_939699.3:n.133G>T
NM_001006657.2:c.100G>T MANE Plus Clinical	NP_001006658.1:p.Glu34Ter
NM_020779.4:c.100G>T MANE Select	NP_065830.2:p.Glu34Ter