Canonical Allele Identifier: CA2624235769

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423490-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423490_23423491insAT , CM000676.2:g.23423490_23423491insAT	GRCh38
NC_000014.8:g.23892699_23892700insAT , CM000676.1:g.23892699_23892700insAT	GRCh37
NC_000014.7:g.22962539_22962540insAT	NCBI36
NG_007884.1:g.17171_17172insAT , LRG_384:g.17171_17172insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+56_3099+57insAT MANE Select	ENSP00000347507.3:n.3099+56_3099+57insAT
ENST00000355349.3:c.3099+56_3099+57insAT	ENSP00000347507.3:n.3099+56_3099+57insAT
NM_000257.3:c.3099+56_3099+57insAT	NP_000248.2:n.3099+56_3099+57insAT
XR_245686.3:n.3205+56_3205+57insAT
XM_017021340.1:c.3099+56_3099+57insAT	XP_016876829.1:n.3099+56_3099+57insAT
NM_000257.4:c.3099+56_3099+57insAT MANE Select	NP_000248.2:n.3099+56_3099+57insAT