Canonical Allele Identifier: CA388981104
Community Standard Title: NM_002471.4(MYH6):c.5792C>T (p.Ala1931Val)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23382432G>A , CM000676.2:g.23382432G>A GRCh38
NC_000014.8:g.23851641G>A , CM000676.1:g.23851641G>A GRCh37
NC_000014.7:g.22921481G>A NCBI36
NG_023444.1:g.30846C>T , LRG_389:g.30846C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.5792C>T MANE Select NP_002462.2:p.Ala1931Val
ENST00000405093.9:c.5792C>T MANE Select ENSP00000386041.3:p.Ala1931Val
NM_002471.3:c.5792C>T , LRG_389t1:c.5792C>T NP_002462.2:p.Ala1931Val
ENST00000356287.3:c.5792C>T ENSP00000348634.3:p.Ala1931Val
ENST00000405093.7:c.5792C>T ENSP00000386041.3:p.Ala1931Val
ENST00000651452.1:n.1019C>T