Canonical Allele Identifier: CA1885485921

Gene: WDR37

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1110170G= , CM000672.2:g.1110170G=	GRCh38
NC_000010.10:g.1156110G= , CM000672.1:g.1156110G=	GRCh37
NC_000010.9:g.1146110G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436154.2:c.1007+4903G=	ENSP00000404346.2:n.1007+4903G=
ENST00000704638.1:c.995+4903G=	ENSP00000515969.1:n.995+4903G=
ENST00000704657.1:c.*946+4903G=	ENSP00000515982.1:n.*946+4903G=
ENST00000704658.1:c.-89+4903G=	ENSP00000515983.1:n.-89+4903G=
ENST00000704671.1:n.2011+4929G=
ENST00000704672.1:c.1080+4929G=	ENSP00000515985.1:n.1080+4929G=
ENST00000704673.1:c.1106+4903G=	ENSP00000515986.1:n.1106+4903G=
ENST00000704674.1:c.-89+4903G=	ENSP00000515987.1:n.-89+4903G=
ENST00000704675.1:n.512+4903G=
ENST00000704738.1:n.1064+4929G=
ENST00000704739.1:c.738+4903G=
ENST00000263150.9:c.1103+4903G= MANE Select	ENSP00000263150.4:n.1103+4903G=
ENST00000650072.1:c.1349+4903G=	ENSP00000497597.1:n.1349+4903G=
ENST00000263150.8:c.1103+4903G=	ENSP00000263150.4:n.1103+4903G=
ENST00000358220.5:c.1103+4903G=	ENSP00000350954.1:n.1103+4903G=
NM_014023.3:c.1103+4903G=	NP_054742.2:n.1103+4903G=
NM_014023.4:c.1103+4903G= MANE Select	NP_054742.2:n.1103+4903G=