Canonical Allele Identifier: CA2123450926

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23422297T= , CM000676.2:g.23422297T=	GRCh38
NC_000014.8:g.23891506T= , CM000676.1:g.23891506T=	GRCh37
NC_000014.7:g.22961346T=	NCBI36
NG_007884.1:g.18365A= , LRG_384:g.18365A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.3128A= MANE Select	ENSP00000347507.3:p.Lys1043=
ENST00000355349.3:c.3128A=	ENSP00000347507.3:p.Lys1043=
NM_000257.3:c.3128A=	NP_000248.2:p.Lys1043=
XR_245686.3:n.3234A=
XM_017021340.1:c.3128A=	XP_016876829.1:p.Lys1043=
NM_000257.4:c.3128A= MANE Select	NP_000248.2:p.Lys1043=