Canonical Allele Identifier: CA2123441801

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417824_23417861delinsGGGCCGAGAACATCAGGCAGAGGATCCCAGCAGGGCGT , CM000676.2:g.23417824_23417861delinsGGGCCGAGAACATCAGGCAGAGGATCCCAGCAGGGCGT	GRCh38
NC_000014.8:g.23887033_23887070delinsGGGCCGAGAACATCAGGCAGAGGATCCCAGCAGGGCGT , CM000676.1:g.23887033_23887070delinsGGGCCGAGAACATCAGGCAGAGGATCCCAGCAGGGCGT	GRCh37
NC_000014.7:g.22956873_22956910delinsGGGCCGAGAACATCAGGCAGAGGATCCCAGCAGGGCGT	NCBI36
NG_007884.1:g.22801_22838delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC , LRG_384:g.22801_22838delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC MANE Select	ENSP00000347507.3:n.4170-175_4170-138delinsACGCCCTGCTGGGATCCT...
ENST00000355349.3:c.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC	ENSP00000347507.3:n.4170-175_4170-138delinsACGCCCTGCTGGGATCCT...
NM_000257.3:c.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC	NP_000248.2:n.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCT...
XM_017021340.1:c.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC	XP_016876829.1:n.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTG...
NM_000257.4:c.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCTGATGTTCTCGGCCC MANE Select	NP_000248.2:n.4170-175_4170-138delinsACGCCCTGCTGGGATCCTCTGCCT...