Canonical Allele Identifier: CA2123453044
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423567G= , CM000676.2:g.23423567G= GRCh38
NC_000014.8:g.23892776G= , CM000676.1:g.23892776G= GRCh37
NC_000014.7:g.22962616G= NCBI36
NG_007884.1:g.17095C= , LRG_384:g.17095C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3079C= MANE Select ENSP00000347507.3:p.Leu1027=
ENST00000355349.3:c.3079C= ENSP00000347507.3:p.Leu1027=
NM_000257.3:c.3079C= NP_000248.2:p.Leu1027=
XR_245686.3:n.3185C=
XM_017021340.1:c.3079C= XP_016876829.1:p.Leu1027=
NM_000257.4:c.3079C= MANE Select NP_000248.2:p.Leu1027=