Canonical Allele Identifier: CA2123465138

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416051C= , CM000676.2:g.23416051C= GRCh38
NC_000014.8:g.23885260C= , CM000676.1:g.23885260C= GRCh37
NC_000014.7:g.22955100C= NCBI36
NG_007884.1:g.24611G= , LRG_384:g.24611G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4906G= (MYH7) MANE Select ENSP00000347507.3:p.Ala1636=
ENST00000355349.3:c.4906G= (MYH7) ENSP00000347507.3:p.Ala1636=
NM_000257.3:c.4906G= (MYH7) NP_000248.2:p.Ala1636=
NR_126491.1:n.312C= (MHRT)
XM_017021340.1:c.4906G= (MYH7) XP_016876829.1:p.Ala1636=
NM_000257.4:c.4906G= (MYH7) MANE Select NP_000248.2:p.Ala1636=