Canonical Allele Identifier: CA2123450648

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431002_23431003delinsGT , CM000676.2:g.23431002_23431003delinsGT	GRCh38
NC_000014.8:g.23900211_23900212delinsGT , CM000676.1:g.23900211_23900212delinsGT	GRCh37
NC_000014.7:g.22970051_22970052delinsGT	NCBI36
NG_007884.1:g.9659_9660delinsAC , LRG_384:g.9659_9660delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-4_797-3delinsAC MANE Select	ENSP00000347507.3:n.797-4_797-3delinsAC
ENST00000355349.3:c.797-4_797-3delinsAC	ENSP00000347507.3:n.797-4_797-3delinsAC
NM_000257.3:c.797-4_797-3delinsAC	NP_000248.2:n.797-4_797-3delinsAC
XR_245686.3:n.903-4_903-3delinsAC
XM_017021340.1:c.797-4_797-3delinsAC	XP_016876829.1:n.797-4_797-3delinsAC
NM_000257.4:c.797-4_797-3delinsAC MANE Select	NP_000248.2:n.797-4_797-3delinsAC