Canonical Allele Identifier: CA345942804

Gene: WDR35

Linked Data

• ClinVar Variation Id: 2938100
• ClinVar RCV Id: RCV003796922
• MyVariant Identifiers: chr2:g.20135219T>G (hg19) ; chr2:g.19935458T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19935458T>G , CM000664.2:g.19935458T>G	GRCh38
NC_000002.11:g.20135219T>G , CM000664.1:g.20135219T>G	GRCh37
NC_000002.10:g.19998700T>G	NCBI36
NG_021212.1:g.59666A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.2547+13A>C MANE Select	ENSP00000281405.5:n.2547+13A>C
ENST00000345530.8:c.2580+13A>C MANE Plus Clinical	ENSP00000314444.5:n.2580+13A>C
ENST00000281405.8:c.2547+13A>C	ENSP00000281405.4:n.2547+13A>C
ENST00000345530.7:c.2580+13A>C	ENSP00000314444.5:n.2580+13A>C
ENST00000414212.5:c.2584+9A>C	ENSP00000390802.1:n.2584+9A>C
ENST00000445063.5:c.2023+13A>C
ENST00000453014.1:c.1198A>C	ENSP00000404409.1:p.Asn400His
NM_001006657.1:c.2580+13A>C	NP_001006658.1:n.2580+13A>C
NM_020779.3:c.2547+13A>C	NP_065830.2:n.2547+13A>C
XM_011533007.1:c.1275+13A>C	XP_011531309.1:n.1275+13A>C
XR_426989.2:n.2580+13A>C
XM_011533007.2:c.1275+13A>C	XP_011531309.1:n.1275+13A>C
XR_001738862.1:n.2524+13A>C
XR_426989.3:n.2580+13A>C
NM_001006657.2:c.2580+13A>C MANE Plus Clinical	NP_001006658.1:n.2580+13A>C
NM_020779.4:c.2547+13A>C MANE Select	NP_065830.2:n.2547+13A>C