Canonical Allele Identifier: CA2588340218

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423436_23423438delinsAAC , CM000676.2:g.23423436_23423438delinsAAC	GRCh38
NC_000014.8:g.23892645_23892647delinsAAC , CM000676.1:g.23892645_23892647delinsAAC	GRCh37
NC_000014.7:g.22962485_22962487delinsAAC	NCBI36
NG_007884.1:g.17224_17226delinsGTT , LRG_384:g.17224_17226delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+109_3099+111delinsGTT MANE Select	ENSP00000347507.3:n.3099+109_3099+111delinsGTT
ENST00000355349.3:c.3099+109_3099+111delinsGTT	ENSP00000347507.3:n.3099+109_3099+111delinsGTT
NM_000257.3:c.3099+109_3099+111delinsGTT	NP_000248.2:n.3099+109_3099+111delinsGTT
XR_245686.3:n.3205+109_3205+111delinsGTT
XM_017021340.1:c.3099+109_3099+111delinsGTT	XP_016876829.1:n.3099+109_3099+111delinsGTT
NM_000257.4:c.3099+109_3099+111delinsGTT MANE Select	NP_000248.2:n.3099+109_3099+111delinsGTT