Canonical Allele Identifier: CA2573149857
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517067
ClinVar RCV Id: RCV002040996
dbSNP Id: rs2138662242

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423541_23423543del , CM000676.2:g.23423541_23423543del GRCh38
NC_000014.8:g.23892750_23892752del , CM000676.1:g.23892750_23892752del GRCh37
NC_000014.7:g.22962590_22962592del NCBI36
NG_007884.1:g.17121_17123del , LRG_384:g.17121_17123del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+6_3099+8del MANE Select ENSP00000347507.3:n.3099+6_3099+8del
ENST00000355349.3:c.3099+6_3099+8del ENSP00000347507.3:n.3099+6_3099+8del
NM_000257.3:c.3099+6_3099+8del NP_000248.2:n.3099+6_3099+8del
XR_245686.3:n.3205+6_3205+8del
XM_017021340.1:c.3099+6_3099+8del XP_016876829.1:n.3099+6_3099+8del
NM_000257.4:c.3099+6_3099+8del MANE Select NP_000248.2:n.3099+6_3099+8del