Canonical Allele Identifier: CA7115226
Community Standard Title: NM_002471.4(MYH6):c.3327A>G (p.Lys1109=)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23392577T>C , CM000676.2:g.23392577T>C GRCh38
NC_000014.8:g.23861786T>C , CM000676.1:g.23861786T>C GRCh37
NC_000014.7:g.22931626T>C NCBI36
NG_023444.1:g.20701A>G , LRG_389:g.20701A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.3327A>G MANE Select NP_002462.2:p.Lys1109=
ENST00000405093.9:c.3327A>G MANE Select ENSP00000386041.3:p.Lys1109=
NM_002471.3:c.3327A>G , LRG_389t1:c.3327A>G NP_002462.2:p.Lys1109=
ENST00000356287.3:c.3327A>G ENSP00000348634.3:p.Lys1109=
ENST00000405093.7:c.3327A>G ENSP00000386041.3:p.Lys1109=