Canonical Allele Identifier: CA345945995

Gene: WDR35

Linked Data

• ClinVar Variation Id: 2949181
• ClinVar RCV Id: RCV003801907
• gnomAD v4: 2-19962329-T-A
• MyVariant Identifiers: chr2:g.20162090T>A (hg19) ; chr2:g.19962329T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19962329T>A , CM000664.2:g.19962329T>A	GRCh38
NC_000002.11:g.20162090T>A , CM000664.1:g.20162090T>A	GRCh37
NC_000002.10:g.20025571T>A	NCBI36
NG_021212.1:g.32795A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.1195-1715A>T MANE Select	ENSP00000281405.5:n.1195-1715A>T
ENST00000345530.8:c.1195-2A>T MANE Plus Clinical	ENSP00000314444.5:n.1195-2A>T
ENST00000281405.8:c.1195-1715A>T	ENSP00000281405.4:n.1195-1715A>T
ENST00000345530.7:c.1195-2A>T	ENSP00000314444.5:n.1195-2A>T
ENST00000414212.5:c.1195-2A>T	ENSP00000390802.1:n.1195-2A>T
ENST00000445063.5:c.731+4395A>T
NM_001006657.1:c.1195-2A>T	NP_001006658.1:n.1195-2A>T
NM_020779.3:c.1195-1715A>T	NP_065830.2:n.1195-1715A>T
XM_011533007.1:c.-18+4395A>T	XP_011531309.1:n.-18+4395A>T
XR_426989.2:n.1228-1715A>T
XR_939699.1:n.1228-1715A>T
XM_011533007.2:c.-18+4395A>T	XP_011531309.1:n.-18+4395A>T
XR_001738862.1:n.1228-1715A>T
XR_426989.3:n.1228-1715A>T
XR_939699.3:n.1228-1715A>T
NM_001006657.2:c.1195-2A>T MANE Plus Clinical	NP_001006658.1:n.1195-2A>T
NM_020779.4:c.1195-1715A>T MANE Select	NP_065830.2:n.1195-1715A>T