Canonical Allele Identifier: CA1232982126

Gene: SH3YL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263489_263517delinsGGGGACCGGCCCTTCCCTTCCGGGTGTGA , CM000664.2:g.263489_263517delinsGGGGACCGGCCCTTCCCTTCCGGGTGTGA	GRCh38
NC_000002.11:g.263489_263517delinsGGGGACCGGCCCTTCCCTTCCGGGTGTGA , CM000664.1:g.263489_263517delinsGGGGACCGGCCCTTCCCTTCCGGGTGTGA	GRCh37
NC_000002.10:g.253489_253517delinsGGGGACCGGCCCTTCCCTTCCGGGTGTGA	NCBI36
NG_012035.1:g.3621_3649delinsGGGGACCGGCCCTTCCCTTCCGGGTGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC MANE Select	ENSP00000348471.5:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGG...
ENST00000356150.9:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000348471.5:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGG...
ENST00000402632.5:c.-155-731_-155-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000384910.1:n.-155-731_-155-703delinsTCACACCCGGAAGGGAAG...
ENST00000403658.5:c.-422+1265_-422+1293delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000383928.1:n.-422+1265_-422+1293delinsTCACACCCGGAAGGGA...
ENST00000403712.6:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000384276.1:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGG...
ENST00000405430.5:c.-281-145_-281-117delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000384269.1:n.-281-145_-281-117delinsTCACACCCGGAAGGGAAG...
ENST00000415368.5:c.-313-149_-313-121delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000410235.1:n.-313-149_-313-121delinsTCACACCCGGAAGGGAAG...
ENST00000454318.1:c.-362+1265_-362+1293delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000415723.1:n.-362+1265_-362+1293delinsTCACACCCGGAAGGGA...
ENST00000462719.1:n.105+2777_106-2769delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000463865.5:n.309+567_309+595delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000465733.5:n.30-145_30-117delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000468321.5:n.42-731_42-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000471948.5:n.467_495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000472861.1:n.30-145_30-117delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000475027.5:n.29+1265_29+1293delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000477707.5:n.228+47_228+75delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000488044.5:n.85+1265_85+1293delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000488979.6:n.27+1025_27+1053delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
ENST00000626873.2:c.-556+627_-556+655delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	ENSP00000485824.1:n.-556+627_-556+655delinsTCACACCCGGAAGGGAAG...
NM_001159597.2:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	NP_001153069.1:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCC...
NM_001282682.1:c.-422+1265_-422+1293delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	NP_001269611.1:n.-422+1265_-422+1293delinsTCACACCCGGAAGGGAAGG...
NM_015677.3:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	NP_056492.2:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NR_104223.1:n.42-731_42-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NR_104224.1:n.86-731_86-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NR_104225.1:n.309+567_309+595delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NM_015677.4:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC MANE Select	NP_056492.2:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NR_104224.2:n.44-731_44-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NM_001159597.3:c.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	NP_001153069.1:n.1+467_1+495delinsTCACACCCGGAAGGGAAGGGCCGGTCC...
NM_001282682.2:c.-422+1265_-422+1293delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC	NP_001269611.1:n.-422+1265_-422+1293delinsTCACACCCGGAAGGGAAGG...
NR_104223.2:n.42-731_42-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC
NR_104224.3:n.44-731_44-703delinsTCACACCCGGAAGGGAAGGGCCGGTCCCC