Canonical Allele Identifier: CA659858679

Gene: WDR37

Linked Data

• dbSNP Id: rs1190906524
• gnomAD v3: 10-1110297-CTCTT-C
• gnomAD v4: 10-1110297-CTCTT-C
• MyVariant Identifiers: chr10:g.1156238_1156241del (hg19) ; chr10:g.1110298_1110301del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1110298_1110301del , CM000672.2:g.1110298_1110301del	GRCh38
NC_000010.10:g.1156238_1156241del , CM000672.1:g.1156238_1156241del	GRCh37
NC_000010.9:g.1146238_1146241del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436154.2:c.1007+5031_1007+5034del	ENSP00000404346.2:n.1007+5031_1007+5034del
ENST00000704638.1:c.995+5031_995+5034del	ENSP00000515969.1:n.995+5031_995+5034del
ENST00000704657.1:c.*946+5031_*946+5034del	ENSP00000515982.1:n.*946+5031_*946+5034del
ENST00000704658.1:c.-89+5031_-89+5034del	ENSP00000515983.1:n.-89+5031_-89+5034del
ENST00000704671.1:n.2011+5057_2011+5060del
ENST00000704672.1:c.1080+5057_1080+5060del	ENSP00000515985.1:n.1080+5057_1080+5060del
ENST00000704673.1:c.1106+5031_1106+5034del	ENSP00000515986.1:n.1106+5031_1106+5034del
ENST00000704674.1:c.-89+5031_-89+5034del	ENSP00000515987.1:n.-89+5031_-89+5034del
ENST00000704675.1:n.512+5031_512+5034del
ENST00000704738.1:n.1064+5057_1064+5060del
ENST00000704739.1:c.738+5031_738+5034del
ENST00000263150.9:c.1103+5031_1103+5034del MANE Select	ENSP00000263150.4:n.1103+5031_1103+5034del
ENST00000650072.1:c.1349+5031_1349+5034del	ENSP00000497597.1:n.1349+5031_1349+5034del
ENST00000263150.8:c.1103+5031_1103+5034del	ENSP00000263150.4:n.1103+5031_1103+5034del
ENST00000358220.5:c.1103+5031_1103+5034del	ENSP00000350954.1:n.1103+5031_1103+5034del
NM_014023.3:c.1103+5031_1103+5034del	NP_054742.2:n.1103+5031_1103+5034del
NM_014023.4:c.1103+5031_1103+5034del MANE Select	NP_054742.2:n.1103+5031_1103+5034del