Canonical Allele Identifier: CA2580069872
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1994344
ClinVar RCV Id: RCV002819016

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859498_46859502delinsCGTGGTGACATGCAGTAATGGTTTGCTGGAGCATCTGGATCCATGCTGATTTGCCAGGCCCCCTGGTGGTAGGCGCTGACACCTATGGAGAAGTGAGAAGGTCGAGTGAG , CM000665.2:g.46859498_46859502delinsCGTGGTGACATGCAGTAATGGTTTGCTGGAGCATCTGGATCCATGCTGATTTGCCAGGCCCCCTGGTGGTAGGCGCTGACACCTATGGAGAAGTGAGAAGGTCGAGTGAG GRCh38
NC_000003.11:g.46900988_46900992delinsCGTGGTGACATGCAGTAATGGTTTGCTGGAGCATCTGGATCCATGCTGATTTGCCAGGCCCCCTGGTGGTAGGCGCTGACACCTATGGAGAAGTGAGAAGGTCGAGTGAG , CM000665.1:g.46900988_46900992delinsCGTGGTGACATGCAGTAATGGTTTGCTGGAGCATCTGGATCCATGCTGATTTGCCAGGCCCCCTGGTGGTAGGCGCTGACACCTATGGAGAAGTGAGAAGGTCGAGTGAG GRCh37
NC_000003.10:g.46875992_46875996delinsCGTGGTGACATGCAGTAATGGTTTGCTGGAGCATCTGGATCCATGCTGATTTGCCAGGCCCCCTGGTGGTAGGCGCTGACACCTATGGAGAAGTGAGAAGGTCGAGTGAG NCBI36
NG_007555.2:g.27668_27672delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG , LRG_395:g.27668_27672delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG

Transcript Alleles

HGVS Amino-acid change
ENST00000431168.2:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG ENSP00000393455.2:p.Glu152_Leu153delinsLe...
ENST00000292327.6:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG MANE Select ENSP00000292327.4:p.Glu152_Leu153delinsLe...
ENST00000653454.1:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG ENSP00000499624.1:p.Glu152_Leu153delinsLe...
ENST00000654597.1:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG ENSP00000499406.1:p.Glu152_Leu153delinsLe...
ENST00000655244.1:n.676_680delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG
ENST00000662933.1:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG ENSP00000499577.1:p.Glu152_Leu153delinsLe...
ENST00000664891.1:n.412_416delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG
ENST00000292327.4:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG ENSP00000292327.4:p.Glu152_Leu153delinsLe...
ENST00000395869.5:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG ENSP00000379210.1:p.Glu152_Leu153delinsLe...
NM_000258.2:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG , LRG_395t1:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG NP_000249.1:p.Glu152_Leu153delinsLeuThrAr...
NM_000258.3:c.454_458delinsCTCACTCGACCTTCTCACTTCTCCATAGGTGTCAGCGCCTACCACCAGGGGGCCTGGCAAATCAGCATGGATCCAGATGCTCCAGCAAACCATTACTGCATGTCACCACG MANE Select NP_000249.1:p.Glu152_Leu153delinsLeuThrAr...