Canonical Allele Identifier: CA2123445172
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429006T= , CM000676.2:g.23429006T= GRCh38
NC_000014.8:g.23898215T= , CM000676.1:g.23898215T= GRCh37
NC_000014.7:g.22968055T= NCBI36
NG_007884.1:g.11656A= , LRG_384:g.11656A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1356A= MANE Select ENSP00000347507.3:p.Pro452=
ENST00000355349.3:c.1356A= ENSP00000347507.3:p.Pro452=
NM_000257.3:c.1356A= NP_000248.2:p.Pro452=
XR_245686.3:n.1462A=
XM_017021340.1:c.1356A= XP_016876829.1:p.Pro452=
NM_000257.4:c.1356A= MANE Select NP_000248.2:p.Pro452=