Canonical Allele Identifier: CA375856303

Gene: WDR37

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1080454C>T , CM000672.2:g.1080454C>T	GRCh38
NC_000010.10:g.1126394C>T , CM000672.1:g.1126394C>T	GRCh37
NC_000010.9:g.1116394C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014023.4:c.374C>T MANE Select	NP_054742.2:p.Thr125Ile
ENST00000263150.9:c.374C>T MANE Select	ENSP00000263150.4:p.Thr125Ile
NM_014023.3:c.374C>T	NP_054742.2:p.Thr125Ile
ENST00000263150.8:c.374C>T	ENSP00000263150.4:p.Thr125Ile
ENST00000358220.5:c.374C>T	ENSP00000350954.1:p.Thr125Ile
ENST00000381329.5:c.374C>T	ENSP00000370730.1:p.Thr125Ile
ENST00000436154.1:c.275C>T	ENSP00000404346.1:p.Thr92Ile
ENST00000436154.2:c.275C>T	ENSP00000404346.2:p.Thr92Ile
ENST00000620998.4:c.374C>T	ENSP00000478057.1:p.Thr125Ile
ENST00000650072.1:c.374C>T	ENSP00000497597.1:p.Thr125Ile
ENST00000704638.1:c.266C>T	ENSP00000515969.1:p.Thr89Ile
ENST00000704657.1:c.*217C>T	ENSP00000515982.1:n.*217C>T
ENST00000704658.1:c.-818C>T	ENSP00000515983.1:n.-818C>T
ENST00000704671.1:n.1308C>T
ENST00000704672.1:c.374C>T	ENSP00000515985.1:p.Thr125Ile
ENST00000704673.1:c.374C>T	ENSP00000515986.1:p.Thr125Ile
ENST00000704674.1:c.-818C>T	ENSP00000515987.1:n.-818C>T
ENST00000704738.1:n.358C>T
ENST00000704739.1:c.244C>T