Canonical Allele Identifier: CA2123468516

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417296T= , CM000676.2:g.23417296T= GRCh38
NC_000014.8:g.23886505T= , CM000676.1:g.23886505T= GRCh37
NC_000014.7:g.22956345T= NCBI36
NG_007884.1:g.23366A= , LRG_384:g.23366A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4376A= (MYH7) MANE Select ENSP00000347507.3:p.Lys1459=
ENST00000355349.3:c.4376A= (MYH7) ENSP00000347507.3:p.Lys1459=
NM_000257.3:c.4376A= (MYH7) NP_000248.2:p.Lys1459=
NR_126491.1:n.736T= (MHRT)
XM_017021340.1:c.4376A= (MYH7) XP_016876829.1:p.Lys1459=
NM_000257.4:c.4376A= (MYH7) MANE Select NP_000248.2:p.Lys1459=