Canonical Allele Identifier: CA2123441496

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417693_23417694delinsAG , CM000676.2:g.23417693_23417694delinsAG	GRCh38
NC_000014.8:g.23886902_23886903delinsAG , CM000676.1:g.23886902_23886903delinsAG	GRCh37
NC_000014.7:g.22956742_22956743delinsAG	NCBI36
NG_007884.1:g.22968_22969delinsCT , LRG_384:g.22968_22969delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-8_4170-7delinsCT MANE Select	ENSP00000347507.3:n.4170-8_4170-7delinsCT
ENST00000355349.3:c.4170-8_4170-7delinsCT	ENSP00000347507.3:n.4170-8_4170-7delinsCT
NM_000257.3:c.4170-8_4170-7delinsCT	NP_000248.2:n.4170-8_4170-7delinsCT
XM_017021340.1:c.4170-8_4170-7delinsCT	XP_016876829.1:n.4170-8_4170-7delinsCT
NM_000257.4:c.4170-8_4170-7delinsCT MANE Select	NP_000248.2:n.4170-8_4170-7delinsCT