Canonical Allele Identifier: CA2123464449

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415783T= , CM000676.2:g.23415783T= GRCh38
NC_000014.8:g.23884992T= , CM000676.1:g.23884992T= GRCh37
NC_000014.7:g.22954832T= NCBI36
NG_007884.1:g.24879A= , LRG_384:g.24879A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5003A= (MYH7) MANE Select ENSP00000347507.3:p.Lys1668=
ENST00000355349.3:c.5003A= (MYH7) ENSP00000347507.3:p.Lys1668=
NM_000257.3:c.5003A= (MYH7) NP_000248.2:p.Lys1668=
NR_126491.1:n.215T= (MHRT)
XM_017021340.1:c.5003A= (MYH7) XP_016876829.1:p.Lys1668=
NM_000257.4:c.5003A= (MYH7) MANE Select NP_000248.2:p.Lys1668=