Canonical Allele Identifier: CA3209385321
Community Standard Title: NM_000257.4(MYH7):c.306C= (p.Leu102=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433123G= , CM000676.2:g.23433123G= GRCh38
NC_000014.8:g.23902332G= , CM000676.1:g.23902332G= GRCh37
NC_000014.7:g.22972172G= NCBI36
NG_007884.1:g.7539C= , LRG_384:g.7539C=

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.306C= MANE Select NP_000248.2:p.Leu102=
ENST00000355349.4:c.306C= MANE Select ENSP00000347507.3:p.Leu102=
NM_000257.3:c.306C= NP_000248.2:p.Leu102=
ENST00000355349.3:c.306C= ENSP00000347507.3:p.Leu102=
XM_017021340.1:c.306C= XP_016876829.1:p.Leu102=
XR_245686.3:n.412C=