Canonical Allele Identifier: CA2123452708

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423430_23423452delinsAACACAAACACACACACACACAC , CM000676.2:g.23423430_23423452delinsAACACAAACACACACACACACAC	GRCh38
NC_000014.8:g.23892639_23892661delinsAACACAAACACACACACACACAC , CM000676.1:g.23892639_23892661delinsAACACAAACACACACACACACAC	GRCh37
NC_000014.7:g.22962479_22962501delinsAACACAAACACACACACACACAC	NCBI36
NG_007884.1:g.17210_17232delinsGTGTGTGTGTGTGTGTTTGTGTT , LRG_384:g.17210_17232delinsGTGTGTGTGTGTGTGTTTGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT MANE Select	ENSP00000347507.3:n.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTG...
ENST00000355349.3:c.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT	ENSP00000347507.3:n.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTG...
NM_000257.3:c.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT	NP_000248.2:n.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT
XR_245686.3:n.3205+95_3205+117delinsGTGTGTGTGTGTGTGTTTGTGTT
XM_017021340.1:c.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT	XP_016876829.1:n.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGT...
NM_000257.4:c.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT MANE Select	NP_000248.2:n.3099+95_3099+117delinsGTGTGTGTGTGTGTGTTTGTGTT