Canonical Allele Identifier: CA1362297665
Gene: MYL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46860771_46860774delinsATCT , CM000665.2:g.46860771_46860774delinsATCT GRCh38
NC_000003.11:g.46902261_46902264delinsATCT , CM000665.1:g.46902261_46902264delinsATCT GRCh37
NC_000003.10:g.46877265_46877268delinsATCT NCBI36
NG_007555.2:g.26396_26399delinsAGAT , LRG_395:g.26396_26399delinsAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000431168.2:c.209_212delinsAGAT ENSP00000393455.2:p.Lys70=
ENST00000292327.6:c.209_212delinsAGAT MANE Select ENSP00000292327.4:p.Lys70=
ENST00000653454.1:c.209_212delinsAGAT ENSP00000499624.1:p.Lys70=
ENST00000654597.1:c.209_212delinsAGAT ENSP00000499406.1:p.Lys70=
ENST00000655244.1:n.431_434delinsAGAT
ENST00000662933.1:c.209_212delinsAGAT ENSP00000499577.1:p.Lys70=
ENST00000664891.1:n.167_170delinsAGAT
ENST00000292327.4:c.209_212delinsAGAT ENSP00000292327.4:p.Lys70=
ENST00000395869.5:c.209_212delinsAGAT ENSP00000379210.1:p.Lys70=
NM_000258.2:c.209_212delinsAGAT , LRG_395t1:c.209_212delinsAGAT NP_000249.1:p.Lys70=
NM_000258.3:c.209_212delinsAGAT MANE Select NP_000249.1:p.Lys70=