Canonical Allele Identifier: CA2800863564

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419474_23419475insCC , CM000676.2:g.23419474_23419475insCC	GRCh38
NC_000014.8:g.23888683_23888684insCC , CM000676.1:g.23888683_23888684insCC	GRCh37
NC_000014.7:g.22958523_22958524insCC	NCBI36
NG_007884.1:g.21187_21188insGG , LRG_384:g.21187_21188insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3853+8_3853+9insGG MANE Select	ENSP00000347507.3:n.3853+8_3853+9insGG
ENST00000355349.3:c.3853+8_3853+9insGG	ENSP00000347507.3:n.3853+8_3853+9insGG
NM_000257.3:c.3853+8_3853+9insGG	NP_000248.2:n.3853+8_3853+9insGG
XM_017021340.1:c.3853+8_3853+9insGG	XP_016876829.1:n.3853+8_3853+9insGG
NM_000257.4:c.3853+8_3853+9insGG MANE Select	NP_000248.2:n.3853+8_3853+9insGG