Canonical Allele Identifier: CA2624254182
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433558_23433559insCC , CM000676.2:g.23433558_23433559insCC GRCh38
NC_000014.8:g.23902767_23902768insCC , CM000676.1:g.23902767_23902768insCC GRCh37
NC_000014.7:g.22972607_22972608insCC NCBI36
NG_007884.1:g.7104_7105insGG , LRG_384:g.7104_7105insGG

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.175_176insGG MANE Select ENSP00000347507.3:p.Val59GlyfsTer12
ENST00000355349.3:c.175_176insGG ENSP00000347507.3:p.Val59GlyfsTer12
NM_000257.3:c.175_176insGG NP_000248.2:p.Val59GlyfsTer12
XR_245686.3:n.281_282insGG
XM_017021340.1:c.175_176insGG XP_016876829.1:p.Val59GlyfsTer12
NM_000257.4:c.175_176insGG MANE Select NP_000248.2:p.Val59GlyfsTer12