Canonical Allele Identifier: CA2123464511

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415795T= , CM000676.2:g.23415795T= GRCh38
NC_000014.8:g.23885004T= , CM000676.1:g.23885004T= GRCh37
NC_000014.7:g.22954844T= NCBI36
NG_007884.1:g.24867A= , LRG_384:g.24867A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4991A= (MYH7) MANE Select ENSP00000347507.3:p.Asn1664=
ENST00000355349.3:c.4991A= (MYH7) ENSP00000347507.3:p.Asn1664=
NM_000257.3:c.4991A= (MYH7) NP_000248.2:p.Asn1664=
NR_126491.1:n.227T= (MHRT)
XM_017021340.1:c.4991A= (MYH7) XP_016876829.1:p.Asn1664=
NM_000257.4:c.4991A= (MYH7) MANE Select NP_000248.2:p.Asn1664=