Canonical Allele Identifier: CA1362297085
Gene: MYL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46859498_46859499delinsAG , CM000665.2:g.46859498_46859499delinsAG GRCh38
NC_000003.11:g.46900988_46900989delinsAG , CM000665.1:g.46900988_46900989delinsAG GRCh37
NC_000003.10:g.46875992_46875993delinsAG NCBI36
NG_007555.2:g.27671_27672delinsCT , LRG_395:g.27671_27672delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000431168.2:c.457_458delinsCT ENSP00000393455.2:p.Leu153=
ENST00000292327.6:c.457_458delinsCT MANE Select ENSP00000292327.4:p.Leu153=
ENST00000653454.1:c.457_458delinsCT ENSP00000499624.1:p.Leu153=
ENST00000654597.1:c.457_458delinsCT ENSP00000499406.1:p.Leu153=
ENST00000655244.1:n.679_680delinsCT
ENST00000662933.1:c.457_458delinsCT ENSP00000499577.1:p.Leu153=
ENST00000664891.1:n.415_416delinsCT
ENST00000292327.4:c.457_458delinsCT ENSP00000292327.4:p.Leu153=
ENST00000395869.5:c.457_458delinsCT ENSP00000379210.1:p.Leu153=
NM_000258.2:c.457_458delinsCT , LRG_395t1:c.457_458delinsCT NP_000249.1:p.Leu153=
NM_000258.3:c.457_458delinsCT MANE Select NP_000249.1:p.Leu153=