Canonical Allele Identifier: CA961074432
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892560389

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423436_23423437insCACACAC , CM000676.2:g.23423436_23423437insCACACAC GRCh38
NC_000014.8:g.23892645_23892646insCACACAC , CM000676.1:g.23892645_23892646insCACACAC GRCh37
NC_000014.7:g.22962485_22962486insCACACAC NCBI36
NG_007884.1:g.17225_17226insGTGTGTG , LRG_384:g.17225_17226insGTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+110_3099+111insGTGTGTG MANE Select ENSP00000347507.3:n.3099+110_3099+111insGTGTGTG
ENST00000355349.3:c.3099+110_3099+111insGTGTGTG ENSP00000347507.3:n.3099+110_3099+111insGTGTGTG
NM_000257.3:c.3099+110_3099+111insGTGTGTG NP_000248.2:n.3099+110_3099+111insGTGTGTG
XR_245686.3:n.3205+110_3205+111insGTGTGTG
XM_017021340.1:c.3099+110_3099+111insGTGTGTG XP_016876829.1:n.3099+110_3099+111insGTGTGTG
NM_000257.4:c.3099+110_3099+111insGTGTGTG MANE Select NP_000248.2:n.3099+110_3099+111insGTGTGTG