Canonical Allele Identifier: CA2624232724

Gene: MYH7

Linked Data

• gnomAD v4: 14-23420869-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420869_23420870insCA , CM000676.2:g.23420869_23420870insCA	GRCh38
NC_000014.8:g.23890078_23890079insCA , CM000676.1:g.23890078_23890079insCA	GRCh37
NC_000014.7:g.22959918_22959919insCA	NCBI36
NG_007884.1:g.19792_19793insTG , LRG_384:g.19792_19793insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+88_3336+89insTG MANE Select	ENSP00000347507.3:n.3336+88_3336+89insTG
ENST00000355349.3:c.3336+88_3336+89insTG	ENSP00000347507.3:n.3336+88_3336+89insTG
NM_000257.3:c.3336+88_3336+89insTG	NP_000248.2:n.3336+88_3336+89insTG
XR_245686.3:n.3444+88_3444+89insTG
XM_017021340.1:c.3336+88_3336+89insTG	XP_016876829.1:n.3336+88_3336+89insTG
NM_000257.4:c.3336+88_3336+89insTG MANE Select	NP_000248.2:n.3336+88_3336+89insTG