Canonical Allele Identifier: CA1232982082

Gene: SH3YL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263426_263443delinsACCCGTGCTCGCCGCGAC , CM000664.2:g.263426_263443delinsACCCGTGCTCGCCGCGAC	GRCh38
NC_000002.11:g.263426_263443delinsACCCGTGCTCGCCGCGAC , CM000664.1:g.263426_263443delinsACCCGTGCTCGCCGCGAC	GRCh37
NC_000002.10:g.253426_253443delinsACCCGTGCTCGCCGCGAC	NCBI36
NG_012035.1:g.3558_3575delinsACCCGTGCTCGCCGCGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT MANE Select	ENSP00000348471.5:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
ENST00000356150.9:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT	ENSP00000348471.5:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
ENST00000402632.5:c.-155-657_-155-640delinsGTCGCGGCGAGCACGGGT	ENSP00000384910.1:n.-155-657_-155-640delinsGTCGCGGCGAGCACGGGT...
ENST00000403658.5:c.-422+1339_-422+1356delinsGTCGCGGCGAGCACGGGT	ENSP00000383928.1:n.-422+1339_-422+1356delinsGTCGCGGCGAGCACGG...
ENST00000403712.6:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT	ENSP00000384276.1:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
ENST00000405430.5:c.-281-71_-281-54delinsGTCGCGGCGAGCACGGGT	ENSP00000384269.1:n.-281-71_-281-54delinsGTCGCGGCGAGCACGGGT
ENST00000415368.5:c.-313-75_-313-58delinsGTCGCGGCGAGCACGGGT	ENSP00000410235.1:n.-313-75_-313-58delinsGTCGCGGCGAGCACGGGT
ENST00000454318.1:c.-362+1339_-362+1356delinsGTCGCGGCGAGCACGGGT	ENSP00000415723.1:n.-362+1339_-362+1356delinsGTCGCGGCGAGCACGG...
ENST00000462719.1:n.106-2723_106-2706delinsGTCGCGGCGAGCACGGGT
ENST00000463865.5:n.309+641_309+658delinsGTCGCGGCGAGCACGGGT
ENST00000465733.5:n.30-71_30-54delinsGTCGCGGCGAGCACGGGT
ENST00000468321.5:n.42-657_42-640delinsGTCGCGGCGAGCACGGGT
ENST00000471948.5:n.541_558delinsGTCGCGGCGAGCACGGGT
ENST00000472861.1:n.30-71_30-54delinsGTCGCGGCGAGCACGGGT
ENST00000475027.5:n.29+1339_29+1356delinsGTCGCGGCGAGCACGGGT
ENST00000477707.5:n.229-71_229-54delinsGTCGCGGCGAGCACGGGT
ENST00000488044.5:n.85+1339_85+1356delinsGTCGCGGCGAGCACGGGT
ENST00000488979.6:n.27+1099_27+1116delinsGTCGCGGCGAGCACGGGT
ENST00000626873.2:c.-556+701_-556+718delinsGTCGCGGCGAGCACGGGT	ENSP00000485824.1:n.-556+701_-556+718delinsGTCGCGGCGAGCACGGGT...
NM_001159597.2:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT	NP_001153069.1:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
NM_001282682.1:c.-422+1339_-422+1356delinsGTCGCGGCGAGCACGGGT	NP_001269611.1:n.-422+1339_-422+1356delinsGTCGCGGCGAGCACGGGT
NM_015677.3:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT	NP_056492.2:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
NR_104223.1:n.42-657_42-640delinsGTCGCGGCGAGCACGGGT
NR_104224.1:n.86-657_86-640delinsGTCGCGGCGAGCACGGGT
NR_104225.1:n.309+641_309+658delinsGTCGCGGCGAGCACGGGT
NM_015677.4:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT MANE Select	NP_056492.2:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
NR_104224.2:n.44-657_44-640delinsGTCGCGGCGAGCACGGGT
NM_001159597.3:c.1+541_1+558delinsGTCGCGGCGAGCACGGGT	NP_001153069.1:n.1+541_1+558delinsGTCGCGGCGAGCACGGGT
NM_001282682.2:c.-422+1339_-422+1356delinsGTCGCGGCGAGCACGGGT	NP_001269611.1:n.-422+1339_-422+1356delinsGTCGCGGCGAGCACGGGT
NR_104223.2:n.42-657_42-640delinsGTCGCGGCGAGCACGGGT
NR_104224.3:n.44-657_44-640delinsGTCGCGGCGAGCACGGGT