Canonical Allele Identifier: CA645591491
Community Standard Title: NM_002471.4(MYH6):c.4593_4594delinsTT (p.Arg1532Cys)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23387585_23387586delinsAA , CM000676.2:g.23387585_23387586delinsAA GRCh38
NC_000014.8:g.23856794_23856795delinsAA , CM000676.1:g.23856794_23856795delinsAA GRCh37
NC_000014.7:g.22926634_22926635delinsAA NCBI36
NG_023444.1:g.25692_25693delinsTT , LRG_389:g.25692_25693delinsTT

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.4593_4594delinsTT MANE Select NP_002462.2:p.Arg1532Cys
ENST00000405093.9:c.4593_4594delinsTT MANE Select ENSP00000386041.3:p.Arg1532Cys
NM_002471.3:c.4593_4594delinsTT , LRG_389t1:c.4593_4594delinsTT NP_002462.2:p.Arg1532Cys
ENST00000356287.3:c.4593_4594delinsTT ENSP00000348634.3:p.Arg1532Cys
ENST00000405093.7:c.4593_4594delinsTT ENSP00000386041.3:p.Arg1532Cys