Canonical Allele Identifier: CA2123464273

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415747A= , CM000676.2:g.23415747A= GRCh38
NC_000014.8:g.23884956A= , CM000676.1:g.23884956A= GRCh37
NC_000014.7:g.22954796A= NCBI36
NG_007884.1:g.24915T= , LRG_384:g.24915T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5039T= (MYH7) MANE Select ENSP00000347507.3:p.Leu1680=
ENST00000355349.3:c.5039T= (MYH7) ENSP00000347507.3:p.Leu1680=
NM_000257.3:c.5039T= (MYH7) NP_000248.2:p.Leu1680=
NR_126491.1:n.179A= (MHRT)
XM_017021340.1:c.5039T= (MYH7) XP_016876829.1:p.Leu1680=
NM_000257.4:c.5039T= (MYH7) MANE Select NP_000248.2:p.Leu1680=