Canonical Allele Identifier: CA2624235680

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423484-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423485_23423486insGA , CM000676.2:g.23423485_23423486insGA	GRCh38
NC_000014.8:g.23892694_23892695insGA , CM000676.1:g.23892694_23892695insGA	GRCh37
NC_000014.7:g.22962534_22962535insGA	NCBI36
NG_007884.1:g.17177_17178insCT , LRG_384:g.17177_17178insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+62_3099+63insCT MANE Select	ENSP00000347507.3:n.3099+62_3099+63insCT
ENST00000355349.3:c.3099+62_3099+63insCT	ENSP00000347507.3:n.3099+62_3099+63insCT
NM_000257.3:c.3099+62_3099+63insCT	NP_000248.2:n.3099+62_3099+63insCT
XR_245686.3:n.3205+62_3205+63insCT
XM_017021340.1:c.3099+62_3099+63insCT	XP_016876829.1:n.3099+62_3099+63insCT
NM_000257.4:c.3099+62_3099+63insCT MANE Select	NP_000248.2:n.3099+62_3099+63insCT