Canonical Allele Identifier: CA2123452883

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423482_23423488delinsCACACAG , CM000676.2:g.23423482_23423488delinsCACACAG	GRCh38
NC_000014.8:g.23892691_23892697delinsCACACAG , CM000676.1:g.23892691_23892697delinsCACACAG	GRCh37
NC_000014.7:g.22962531_22962537delinsCACACAG	NCBI36
NG_007884.1:g.17174_17180delinsCTGTGTG , LRG_384:g.17174_17180delinsCTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+59_3099+65delinsCTGTGTG MANE Select	ENSP00000347507.3:n.3099+59_3099+65delinsCTGTGTG
ENST00000355349.3:c.3099+59_3099+65delinsCTGTGTG	ENSP00000347507.3:n.3099+59_3099+65delinsCTGTGTG
NM_000257.3:c.3099+59_3099+65delinsCTGTGTG	NP_000248.2:n.3099+59_3099+65delinsCTGTGTG
XR_245686.3:n.3205+59_3205+65delinsCTGTGTG
XM_017021340.1:c.3099+59_3099+65delinsCTGTGTG	XP_016876829.1:n.3099+59_3099+65delinsCTGTGTG
NM_000257.4:c.3099+59_3099+65delinsCTGTGTG MANE Select	NP_000248.2:n.3099+59_3099+65delinsCTGTGTG