Canonical Allele Identifier: CA2123456436

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433937_23433941delinsCAACT , CM000676.2:g.23433937_23433941delinsCAACT	GRCh38
NC_000014.8:g.23903146_23903150delinsCAACT , CM000676.1:g.23903146_23903150delinsCAACT	GRCh37
NC_000014.7:g.22972986_22972990delinsCAACT	NCBI36
NG_007884.1:g.6721_6725delinsAGTTG , LRG_384:g.6721_6725delinsAGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.-8-201_-8-197delinsAGTTG MANE Select	ENSP00000347507.3:n.-8-201_-8-197delinsAGTTG
ENST00000355349.3:c.-8-201_-8-197delinsAGTTG	ENSP00000347507.3:n.-8-201_-8-197delinsAGTTG
NM_000257.3:c.-8-201_-8-197delinsAGTTG	NP_000248.2:n.-8-201_-8-197delinsAGTTG
XR_245686.3:n.99-201_99-197delinsAGTTG
XM_017021340.1:c.-8-201_-8-197delinsAGTTG	XP_016876829.1:n.-8-201_-8-197delinsAGTTG
NM_000257.4:c.-8-201_-8-197delinsAGTTG MANE Select	NP_000248.2:n.-8-201_-8-197delinsAGTTG