Canonical Allele Identifier: CA2695224337
Gene: MYH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639353_10639356delinsAACAAATTGA , CM000679.2:g.10639353_10639356delinsAACAAATTGA GRCh38
NC_000017.10:g.10542670_10542673delinsAACAAATTGA , CM000679.1:g.10542670_10542673delinsAACAAATTGA GRCh37
NC_000017.9:g.10483395_10483398delinsAACAAATTGA NCBI36
NG_011537.1:g.22943_22946delinsTCAATTTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.3044_3047delinsTCAATTTGTT MANE Select ENSP00000464317.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
ENST00000583535.5:c.3044_3047delinsTCAATTTGTT ENSP00000464317.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
NM_002470.3:c.3044_3047delinsTCAATTTGTT NP_002461.2:p.Glu1015_Asp1016delinsValAsnLeuPhe
XM_011523870.1:c.3044_3047delinsTCAATTTGTT XP_011522172.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
XM_011523871.1:c.3044_3047delinsTCAATTTGTT XP_011522173.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
XM_011523872.1:c.3044_3047delinsTCAATTTGTT XP_011522174.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
XM_011523870.3:c.3044_3047delinsTCAATTTGTT XP_011522172.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
XM_011523871.2:c.3044_3047delinsTCAATTTGTT XP_011522173.1:p.Glu1015_Asp1016delinsValAsnLeuPhe
NM_002470.4:c.3044_3047delinsTCAATTTGTT MANE Select NP_002461.2:p.Glu1015_Asp1016delinsValAsnLeuPhe