Canonical Allele Identifier: CA2624237987
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424216_23424225del , CM000676.2:g.23424216_23424225del GRCh38
NC_000014.8:g.23893425_23893434del , CM000676.1:g.23893425_23893434del GRCh37
NC_000014.7:g.22963265_22963274del NCBI36
NG_007884.1:g.16438_16447del , LRG_384:g.16438_16447del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-75_2680-66del MANE Select ENSP00000347507.3:n.2680-75_2680-66del
ENST00000355349.3:c.2680-75_2680-66del ENSP00000347507.3:n.2680-75_2680-66del
NM_000257.3:c.2680-75_2680-66del NP_000248.2:n.2680-75_2680-66del
XR_245686.3:n.2786-75_2786-66del
XM_017021340.1:c.2680-75_2680-66del XP_016876829.1:n.2680-75_2680-66del
NM_000257.4:c.2680-75_2680-66del MANE Select NP_000248.2:n.2680-75_2680-66del