Canonical Allele Identifier: CA2800863603
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419686_23419687insTCCTGTCCAGGGATGCAGCAGAAGC , CM000676.2:g.23419686_23419687insTCCTGTCCAGGGATGCAGCAGAAGC GRCh38
NC_000014.8:g.23888895_23888896insTCCTGTCCAGGGATGCAGCAGAAGC , CM000676.1:g.23888895_23888896insTCCTGTCCAGGGATGCAGCAGAAGC GRCh37
NC_000014.7:g.22958735_22958736insTCCTGTCCAGGGATGCAGCAGAAGC NCBI36
NG_007884.1:g.20975_20976insGCTTCTGCTGCATCCCTGGACAGGA , LRG_384:g.20975_20976insGCTTCTGCTGCATCCCTGGACAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA MANE Select ENSP00000347507.3:n.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAG...
ENST00000355349.3:c.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA ENSP00000347507.3:n.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAG...
NM_000257.3:c.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA NP_000248.2:n.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA
XM_017021340.1:c.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA XP_016876829.1:n.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA
NM_000257.4:c.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA MANE Select NP_000248.2:n.3727-78_3727-77insGCTTCTGCTGCATCCCTGGACAGGA