Canonical Allele Identifier: CA2559599760

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23429187_23429188insGGA , CM000676.2:g.23429187_23429188insGGA	GRCh38
NC_000014.8:g.23898396_23898397insGGA , CM000676.1:g.23898396_23898397insGGA	GRCh37
NC_000014.7:g.22968236_22968237insGGA	NCBI36
NG_007884.1:g.11474_11475insTCC , LRG_384:g.11474_11475insTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.1257+41_1257+42insTCC MANE Select	ENSP00000347507.3:n.1257+41_1257+42insTCC
ENST00000355349.3:c.1257+41_1257+42insTCC	ENSP00000347507.3:n.1257+41_1257+42insTCC
NM_000257.3:c.1257+41_1257+42insTCC	NP_000248.2:n.1257+41_1257+42insTCC
XR_245686.3:n.1363+41_1363+42insTCC
XM_017021340.1:c.1257+41_1257+42insTCC	XP_016876829.1:n.1257+41_1257+42insTCC
NM_000257.4:c.1257+41_1257+42insTCC MANE Select	NP_000248.2:n.1257+41_1257+42insTCC