Canonical Allele Identifier: CA2123450949
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892920828

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431192_23431193del , CM000676.2:g.23431192_23431193del GRCh38
NC_000014.8:g.23900401_23900402del , CM000676.1:g.23900401_23900402del GRCh37
NC_000014.7:g.22970241_22970242del NCBI36
NG_007884.1:g.9470_9471del , LRG_384:g.9470_9471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-193_797-192del MANE Select ENSP00000347507.3:n.797-193_797-192del
ENST00000355349.3:c.797-193_797-192del ENSP00000347507.3:n.797-193_797-192del
NM_000257.3:c.797-193_797-192del NP_000248.2:n.797-193_797-192del
XR_245686.3:n.903-193_903-192del
XM_017021340.1:c.797-193_797-192del XP_016876829.1:n.797-193_797-192del
NM_000257.4:c.797-193_797-192del MANE Select NP_000248.2:n.797-193_797-192del