Canonical Allele Identifier: CA1232982044

Gene: SH3YL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263376_263379delinsAAAG , CM000664.2:g.263376_263379delinsAAAG	GRCh38
NC_000002.11:g.263376_263379delinsAAAG , CM000664.1:g.263376_263379delinsAAAG	GRCh37
NC_000002.10:g.253376_253379delinsAAAG	NCBI36
NG_012035.1:g.3508_3511delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+605_1+608delinsCTTT MANE Select	ENSP00000348471.5:n.1+605_1+608delinsCTTT
ENST00000356150.9:c.1+605_1+608delinsCTTT	ENSP00000348471.5:n.1+605_1+608delinsCTTT
ENST00000402632.5:c.-155-593_-155-590delinsCTTT	ENSP00000384910.1:n.-155-593_-155-590delinsCTTT
ENST00000403658.5:c.-422+1403_-422+1406delinsCTTT	ENSP00000383928.1:n.-422+1403_-422+1406delinsCTTT
ENST00000403712.6:c.1+605_1+608delinsCTTT	ENSP00000384276.1:n.1+605_1+608delinsCTTT
ENST00000405430.5:c.-281-7_-281-4delinsCTTT	ENSP00000384269.1:n.-281-7_-281-4delinsCTTT
ENST00000415368.5:c.-313-11_-313-8delinsCTTT	ENSP00000410235.1:n.-313-11_-313-8delinsCTTT
ENST00000454318.1:c.-362+1403_-362+1406delinsCTTT	ENSP00000415723.1:n.-362+1403_-362+1406delinsCTTT
ENST00000462719.1:n.106-2659_106-2656delinsCTTT
ENST00000463865.5:n.309+705_309+708delinsCTTT
ENST00000465733.5:n.30-7_30-4delinsCTTT
ENST00000468321.5:n.42-593_42-590delinsCTTT
ENST00000471948.5:n.605_608delinsCTTT
ENST00000472861.1:n.30-7_30-4delinsCTTT
ENST00000475027.5:n.29+1403_29+1406delinsCTTT
ENST00000477707.5:n.229-7_229-4delinsCTTT
ENST00000488044.5:n.85+1403_85+1406delinsCTTT
ENST00000488979.6:n.27+1163_27+1166delinsCTTT
ENST00000626873.2:c.-556+765_-556+768delinsCTTT	ENSP00000485824.1:n.-556+765_-556+768delinsCTTT
NM_001159597.2:c.1+605_1+608delinsCTTT	NP_001153069.1:n.1+605_1+608delinsCTTT
NM_001282682.1:c.-422+1403_-422+1406delinsCTTT	NP_001269611.1:n.-422+1403_-422+1406delinsCTTT
NM_015677.3:c.1+605_1+608delinsCTTT	NP_056492.2:n.1+605_1+608delinsCTTT
NR_104223.1:n.42-593_42-590delinsCTTT
NR_104224.1:n.86-593_86-590delinsCTTT
NR_104225.1:n.309+705_309+708delinsCTTT
NM_015677.4:c.1+605_1+608delinsCTTT MANE Select	NP_056492.2:n.1+605_1+608delinsCTTT
NR_104224.2:n.44-593_44-590delinsCTTT
NM_001159597.3:c.1+605_1+608delinsCTTT	NP_001153069.1:n.1+605_1+608delinsCTTT
NM_001282682.2:c.-422+1403_-422+1406delinsCTTT	NP_001269611.1:n.-422+1403_-422+1406delinsCTTT
NR_104223.2:n.42-593_42-590delinsCTTT
NR_104224.3:n.44-593_44-590delinsCTTT