Canonical Allele Identifier: CA7114828
Community Standard Title: NM_002471.4(MYH6):c.4299C>T (p.Asp1433=)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23388215G>A , CM000676.2:g.23388215G>A GRCh38
NC_000014.8:g.23857424G>A , CM000676.1:g.23857424G>A GRCh37
NC_000014.7:g.22927264G>A NCBI36
NG_023444.1:g.25063C>T , LRG_389:g.25063C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.4299C>T MANE Select NP_002462.2:p.Asp1433=
ENST00000405093.9:c.4299C>T MANE Select ENSP00000386041.3:p.Asp1433=
NM_002471.3:c.4299C>T , LRG_389t1:c.4299C>T NP_002462.2:p.Asp1433=
ENST00000356287.3:c.4299C>T ENSP00000348634.3:p.Asp1433=
ENST00000405093.7:c.4299C>T ENSP00000386041.3:p.Asp1433=