Canonical Allele Identifier: CA2657617060

Gene: SH3YL1

Linked Data

• gnomAD v4: 2-263402-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263404del , CM000664.2:g.263404del	GRCh38
NC_000002.11:g.263404del , CM000664.1:g.263404del	GRCh37
NC_000002.10:g.253404del	NCBI36
NG_012035.1:g.3536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+581del MANE Select	ENSP00000348471.5:n.1+581del
ENST00000356150.9:c.1+581del	ENSP00000348471.5:n.1+581del
ENST00000402632.5:c.-155-617del	ENSP00000384910.1:n.-155-617del
ENST00000403658.5:c.-422+1379del	ENSP00000383928.1:n.-422+1379del
ENST00000403712.6:c.1+581del	ENSP00000384276.1:n.1+581del
ENST00000405430.5:c.-281-31del	ENSP00000384269.1:n.-281-31del
ENST00000415368.5:c.-313-35del	ENSP00000410235.1:n.-313-35del
ENST00000454318.1:c.-362+1379del	ENSP00000415723.1:n.-362+1379del
ENST00000462719.1:n.106-2683del
ENST00000463865.5:n.309+681del
ENST00000465733.5:n.30-31del
ENST00000468321.5:n.42-617del
ENST00000471948.5:n.581del
ENST00000472861.1:n.30-31del
ENST00000475027.5:n.29+1379del
ENST00000477707.5:n.229-31del
ENST00000488044.5:n.85+1379del
ENST00000488979.6:n.27+1139del
ENST00000626873.2:c.-556+741del	ENSP00000485824.1:n.-556+741del
NM_001159597.2:c.1+581del	NP_001153069.1:n.1+581del
NM_001282682.1:c.-422+1379del	NP_001269611.1:n.-422+1379del
NM_015677.3:c.1+581del	NP_056492.2:n.1+581del
NR_104223.1:n.42-617del
NR_104224.1:n.86-617del
NR_104225.1:n.309+681del
NM_015677.4:c.1+581del MANE Select	NP_056492.2:n.1+581del
NR_104224.2:n.44-617del
NM_001159597.3:c.1+581del	NP_001153069.1:n.1+581del
NM_001282682.2:c.-422+1379del	NP_001269611.1:n.-422+1379del
NR_104223.2:n.42-617del
NR_104224.3:n.44-617del