Canonical Allele Identifier: CA2123464413

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415775T= , CM000676.2:g.23415775T= GRCh38
NC_000014.8:g.23884984T= , CM000676.1:g.23884984T= GRCh37
NC_000014.7:g.22954824T= NCBI36
NG_007884.1:g.24887A= , LRG_384:g.24887A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5011A= (MYH7) MANE Select ENSP00000347507.3:p.Ile1671=
ENST00000355349.3:c.5011A= (MYH7) ENSP00000347507.3:p.Ile1671=
NM_000257.3:c.5011A= (MYH7) NP_000248.2:p.Ile1671=
NR_126491.1:n.207T= (MHRT)
XM_017021340.1:c.5011A= (MYH7) XP_016876829.1:p.Ile1671=
NM_000257.4:c.5011A= (MYH7) MANE Select NP_000248.2:p.Ile1671=