Canonical Allele Identifier: CA389053533
Community Standard Title: NM_000257.4(MYH7):c.203C>A (p.Thr68Lys)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433226G>T , CM000676.2:g.23433226G>T GRCh38
NC_000014.8:g.23902435G>T , CM000676.1:g.23902435G>T GRCh37
NC_000014.7:g.22972275G>T NCBI36
NG_007884.1:g.7436C>A , LRG_384:g.7436C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.203C>A MANE Select NP_000248.2:p.Thr68Lys
ENST00000355349.4:c.203C>A MANE Select ENSP00000347507.3:p.Thr68Lys
NM_000257.3:c.203C>A NP_000248.2:p.Thr68Lys
ENST00000355349.3:c.203C>A ENSP00000347507.3:p.Thr68Lys
XM_017021340.1:c.203C>A XP_016876829.1:p.Thr68Lys
XR_245686.3:n.309C>A