Canonical Allele Identifier: CA1542842

Gene: WDR35

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19932317T>C , CM000664.2:g.19932317T>C	GRCh38
NC_000002.11:g.20132078T>C , CM000664.1:g.20132078T>C	GRCh37
NC_000002.10:g.19995559T>C	NCBI36
NG_021212.1:g.62807A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020779.4:c.2789A>G MANE Select	NP_065830.2:p.Asn930Ser
ENST00000281405.9:c.2789A>G MANE Select	ENSP00000281405.5:p.Asn930Ser
NM_001006657.2:c.2822A>G MANE Plus Clinical	NP_001006658.1:p.Asn941Ser
ENST00000345530.8:c.2822A>G MANE Plus Clinical	ENSP00000314444.5:p.Asn941Ser
NM_001006657.1:c.2822A>G	NP_001006658.1:p.Asn941Ser
NM_020779.3:c.2789A>G	NP_065830.2:p.Asn930Ser
ENST00000281405.8:c.2789A>G	ENSP00000281405.4:p.Asn930Ser
ENST00000345530.7:c.2822A>G	ENSP00000314444.5:p.Asn941Ser
ENST00000414212.5:c.*138+66A>G	ENSP00000390802.1:n.*138+66A>G
ENST00000445063.5:c.2024-908A>G
XM_011533007.1:c.1517A>G	XP_011531309.1:p.Asn506Ser
XM_011533007.2:c.1517A>G	XP_011531309.1:p.Asn506Ser
XR_426989.2:n.2756+66A>G
XR_426989.3:n.2756+66A>G