Canonical Allele Identifier: CA1885485909

Gene: WDR37

Linked Data

• dbSNP Id: rs1835164764

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1110144_1110145del , CM000672.2:g.1110144_1110145del	GRCh38
NC_000010.10:g.1156084_1156085del , CM000672.1:g.1156084_1156085del	GRCh37
NC_000010.9:g.1146084_1146085del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436154.2:c.1007+4877_1007+4878del	ENSP00000404346.2:n.1007+4877_1007+4878del
ENST00000704638.1:c.995+4877_995+4878del	ENSP00000515969.1:n.995+4877_995+4878del
ENST00000704657.1:c.*946+4877_*946+4878del	ENSP00000515982.1:n.*946+4877_*946+4878del
ENST00000704658.1:c.-89+4877_-89+4878del	ENSP00000515983.1:n.-89+4877_-89+4878del
ENST00000704671.1:n.2011+4903_2011+4904del
ENST00000704672.1:c.1080+4903_1080+4904del	ENSP00000515985.1:n.1080+4903_1080+4904del
ENST00000704673.1:c.1106+4877_1106+4878del	ENSP00000515986.1:n.1106+4877_1106+4878del
ENST00000704674.1:c.-89+4877_-89+4878del	ENSP00000515987.1:n.-89+4877_-89+4878del
ENST00000704675.1:n.512+4877_512+4878del
ENST00000704738.1:n.1064+4903_1064+4904del
ENST00000704739.1:c.738+4877_738+4878del
ENST00000263150.9:c.1103+4877_1103+4878del MANE Select	ENSP00000263150.4:n.1103+4877_1103+4878del
ENST00000650072.1:c.1349+4877_1349+4878del	ENSP00000497597.1:n.1349+4877_1349+4878del
ENST00000263150.8:c.1103+4877_1103+4878del	ENSP00000263150.4:n.1103+4877_1103+4878del
ENST00000358220.5:c.1103+4877_1103+4878del	ENSP00000350954.1:n.1103+4877_1103+4878del
NM_014023.3:c.1103+4877_1103+4878del	NP_054742.2:n.1103+4877_1103+4878del
NM_014023.4:c.1103+4877_1103+4878del MANE Select	NP_054742.2:n.1103+4877_1103+4878del