Canonical Allele Identifier: CA1232982077

Gene: SH3YL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263418_263420delinsCAG , CM000664.2:g.263418_263420delinsCAG	GRCh38
NC_000002.11:g.263418_263420delinsCAG , CM000664.1:g.263418_263420delinsCAG	GRCh37
NC_000002.10:g.253418_253420delinsCAG	NCBI36
NG_012035.1:g.3550_3552delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+564_1+566delinsCTG MANE Select	ENSP00000348471.5:n.1+564_1+566delinsCTG
ENST00000356150.9:c.1+564_1+566delinsCTG	ENSP00000348471.5:n.1+564_1+566delinsCTG
ENST00000402632.5:c.-155-634_-155-632delinsCTG	ENSP00000384910.1:n.-155-634_-155-632delinsCTG
ENST00000403658.5:c.-422+1362_-422+1364delinsCTG	ENSP00000383928.1:n.-422+1362_-422+1364delinsCTG
ENST00000403712.6:c.1+564_1+566delinsCTG	ENSP00000384276.1:n.1+564_1+566delinsCTG
ENST00000405430.5:c.-281-48_-281-46delinsCTG	ENSP00000384269.1:n.-281-48_-281-46delinsCTG
ENST00000415368.5:c.-313-52_-313-50delinsCTG	ENSP00000410235.1:n.-313-52_-313-50delinsCTG
ENST00000454318.1:c.-362+1362_-362+1364delinsCTG	ENSP00000415723.1:n.-362+1362_-362+1364delinsCTG
ENST00000462719.1:n.106-2700_106-2698delinsCTG
ENST00000463865.5:n.309+664_309+666delinsCTG
ENST00000465733.5:n.30-48_30-46delinsCTG
ENST00000468321.5:n.42-634_42-632delinsCTG
ENST00000471948.5:n.564_566delinsCTG
ENST00000472861.1:n.30-48_30-46delinsCTG
ENST00000475027.5:n.29+1362_29+1364delinsCTG
ENST00000477707.5:n.229-48_229-46delinsCTG
ENST00000488044.5:n.85+1362_85+1364delinsCTG
ENST00000488979.6:n.27+1122_27+1124delinsCTG
ENST00000626873.2:c.-556+724_-556+726delinsCTG	ENSP00000485824.1:n.-556+724_-556+726delinsCTG
NM_001159597.2:c.1+564_1+566delinsCTG	NP_001153069.1:n.1+564_1+566delinsCTG
NM_001282682.1:c.-422+1362_-422+1364delinsCTG	NP_001269611.1:n.-422+1362_-422+1364delinsCTG
NM_015677.3:c.1+564_1+566delinsCTG	NP_056492.2:n.1+564_1+566delinsCTG
NR_104223.1:n.42-634_42-632delinsCTG
NR_104224.1:n.86-634_86-632delinsCTG
NR_104225.1:n.309+664_309+666delinsCTG
NM_015677.4:c.1+564_1+566delinsCTG MANE Select	NP_056492.2:n.1+564_1+566delinsCTG
NR_104224.2:n.44-634_44-632delinsCTG
NM_001159597.3:c.1+564_1+566delinsCTG	NP_001153069.1:n.1+564_1+566delinsCTG
NM_001282682.2:c.-422+1362_-422+1364delinsCTG	NP_001269611.1:n.-422+1362_-422+1364delinsCTG
NR_104223.2:n.42-634_42-632delinsCTG
NR_104224.3:n.44-634_44-632delinsCTG