Canonical Allele Identifier: CA1232982030

Gene: SH3YL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263351A= , CM000664.2:g.263351A=	GRCh38
NC_000002.11:g.263351A= , CM000664.1:g.263351A=	GRCh37
NC_000002.10:g.253351A=	NCBI36
NG_012035.1:g.3483A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+633T= MANE Select	ENSP00000348471.5:n.1+633T=
ENST00000356150.9:c.1+633T=	ENSP00000348471.5:n.1+633T=
ENST00000402632.5:c.-155-565T=	ENSP00000384910.1:n.-155-565T=
ENST00000403658.5:c.-422+1431T=	ENSP00000383928.1:n.-422+1431T=
ENST00000403712.6:c.1+633T=	ENSP00000384276.1:n.1+633T=
ENST00000405430.5:c.-260T=	ENSP00000384269.1:n.-260T=
ENST00000415368.5:c.-296T=	ENSP00000410235.1:n.-296T=
ENST00000454318.1:c.-362+1431T=	ENSP00000415723.1:n.-362+1431T=
ENST00000462719.1:n.106-2631T=
ENST00000463865.5:n.309+733T=
ENST00000465733.5:n.51T=
ENST00000468321.5:n.42-565T=
ENST00000471948.5:n.633T=
ENST00000472861.1:n.51T=
ENST00000475027.5:n.29+1431T=
ENST00000477707.5:n.250T=
ENST00000488044.5:n.85+1431T=
ENST00000488979.6:n.27+1191T=
ENST00000626873.2:c.-556+793T=	ENSP00000485824.1:n.-556+793T=
NM_001159597.2:c.1+633T=	NP_001153069.1:n.1+633T=
NM_001282682.1:c.-422+1431T=	NP_001269611.1:n.-422+1431T=
NM_015677.3:c.1+633T=	NP_056492.2:n.1+633T=
NR_104223.1:n.42-565T=
NR_104224.1:n.86-565T=
NR_104225.1:n.309+733T=
NM_015677.4:c.1+633T= MANE Select	NP_056492.2:n.1+633T=
NR_104224.2:n.44-565T=
NM_001159597.3:c.1+633T=	NP_001153069.1:n.1+633T=
NM_001282682.2:c.-422+1431T=	NP_001269611.1:n.-422+1431T=
NR_104223.2:n.42-565T=
NR_104224.3:n.44-565T=