Canonical Allele Identifier: CA2748574094

Gene: SH3YL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.263474_263475insCGAGGGCGTACCT , CM000664.2:g.263474_263475insCGAGGGCGTACCT	GRCh38
NC_000002.11:g.263474_263475insCGAGGGCGTACCT , CM000664.1:g.263474_263475insCGAGGGCGTACCT	GRCh37
NC_000002.10:g.253474_253475insCGAGGGCGTACCT	NCBI36
NG_012035.1:g.3606_3607insCGAGGGCGTACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356150.10:c.1+509_1+510insAGGTACGCCCTCG MANE Select	ENSP00000348471.5:n.1+509_1+510insAGGTACGCCCTCG
ENST00000356150.9:c.1+509_1+510insAGGTACGCCCTCG	ENSP00000348471.5:n.1+509_1+510insAGGTACGCCCTCG
ENST00000402632.5:c.-155-689_-155-688insAGGTACGCCCTCG	ENSP00000384910.1:n.-155-689_-155-688insAGGTACGCCCTCG
ENST00000403658.5:c.-422+1307_-422+1308insAGGTACGCCCTCG	ENSP00000383928.1:n.-422+1307_-422+1308insAGGTACGCCCTCG
ENST00000403712.6:c.1+509_1+510insAGGTACGCCCTCG	ENSP00000384276.1:n.1+509_1+510insAGGTACGCCCTCG
ENST00000405430.5:c.-281-103_-281-102insAGGTACGCCCTCG	ENSP00000384269.1:n.-281-103_-281-102insAGGTACGCCCTCG
ENST00000415368.5:c.-313-107_-313-106insAGGTACGCCCTCG	ENSP00000410235.1:n.-313-107_-313-106insAGGTACGCCCTCG
ENST00000454318.1:c.-362+1307_-362+1308insAGGTACGCCCTCG	ENSP00000415723.1:n.-362+1307_-362+1308insAGGTACGCCCTCG
ENST00000462719.1:n.106-2755_106-2754insAGGTACGCCCTCG
ENST00000463865.5:n.309+609_309+610insAGGTACGCCCTCG
ENST00000465733.5:n.30-103_30-102insAGGTACGCCCTCG
ENST00000468321.5:n.42-689_42-688insAGGTACGCCCTCG
ENST00000471948.5:n.509_510insAGGTACGCCCTCG
ENST00000472861.1:n.30-103_30-102insAGGTACGCCCTCG
ENST00000475027.5:n.29+1307_29+1308insAGGTACGCCCTCG
ENST00000477707.5:n.228+89_228+90insAGGTACGCCCTCG
ENST00000488044.5:n.85+1307_85+1308insAGGTACGCCCTCG
ENST00000488979.6:n.27+1067_27+1068insAGGTACGCCCTCG
ENST00000626873.2:c.-556+669_-556+670insAGGTACGCCCTCG	ENSP00000485824.1:n.-556+669_-556+670insAGGTACGCCCTCG
NM_001159597.2:c.1+509_1+510insAGGTACGCCCTCG	NP_001153069.1:n.1+509_1+510insAGGTACGCCCTCG
NM_001282682.1:c.-422+1307_-422+1308insAGGTACGCCCTCG	NP_001269611.1:n.-422+1307_-422+1308insAGGTACGCCCTCG
NM_015677.3:c.1+509_1+510insAGGTACGCCCTCG	NP_056492.2:n.1+509_1+510insAGGTACGCCCTCG
NR_104223.1:n.42-689_42-688insAGGTACGCCCTCG
NR_104224.1:n.86-689_86-688insAGGTACGCCCTCG
NR_104225.1:n.309+609_309+610insAGGTACGCCCTCG
NM_015677.4:c.1+509_1+510insAGGTACGCCCTCG MANE Select	NP_056492.2:n.1+509_1+510insAGGTACGCCCTCG
NR_104224.2:n.44-689_44-688insAGGTACGCCCTCG
NM_001159597.3:c.1+509_1+510insAGGTACGCCCTCG	NP_001153069.1:n.1+509_1+510insAGGTACGCCCTCG
NM_001282682.2:c.-422+1307_-422+1308insAGGTACGCCCTCG	NP_001269611.1:n.-422+1307_-422+1308insAGGTACGCCCTCG
NR_104223.2:n.42-689_42-688insAGGTACGCCCTCG
NR_104224.3:n.44-689_44-688insAGGTACGCCCTCG