Canonical Allele Identifier: CA2123446581

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23429550C= , CM000676.2:g.23429550C=	GRCh38
NC_000014.8:g.23898759C= , CM000676.1:g.23898759C=	GRCh37
NC_000014.7:g.22968599C=	NCBI36
NG_007884.1:g.11112G= , LRG_384:g.11112G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.1139-203G= MANE Select	ENSP00000347507.3:n.1139-203G=
ENST00000355349.3:c.1139-203G=	ENSP00000347507.3:n.1139-203G=
NM_000257.3:c.1139-203G=	NP_000248.2:n.1139-203G=
XR_245686.3:n.1245-203G=
XM_017021340.1:c.1139-203G=	XP_016876829.1:n.1139-203G=
NM_000257.4:c.1139-203G= MANE Select	NP_000248.2:n.1139-203G=