Canonical Allele Identifier: CA961074372

Gene: MYH7

Linked Data

• dbSNP Id: rs1892560389
• gnomAD v3: 14-23423436-A-ACACACACAC
• gnomAD v4: 14-23423436-A-ACACACACAC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423436_23423437insCACACACAC , CM000676.2:g.23423436_23423437insCACACACAC	GRCh38
NC_000014.8:g.23892645_23892646insCACACACAC , CM000676.1:g.23892645_23892646insCACACACAC	GRCh37
NC_000014.7:g.22962485_22962486insCACACACAC	NCBI36
NG_007884.1:g.17225_17226insGTGTGTGTG , LRG_384:g.17225_17226insGTGTGTGTG

Transcript Alleles

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