Canonical Allele Identifier: CA2123457930

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425553_23425554delinsAG , CM000676.2:g.23425553_23425554delinsAG	GRCh38
NC_000014.8:g.23894762_23894763delinsAG , CM000676.1:g.23894762_23894763delinsAG	GRCh37
NC_000014.7:g.22964602_22964603delinsAG	NCBI36
NG_007884.1:g.15108_15109delinsCT , LRG_384:g.15108_15109delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2287-136_2287-135delinsCT MANE Select	ENSP00000347507.3:n.2287-136_2287-135delinsCT
ENST00000355349.3:c.2287-136_2287-135delinsCT	ENSP00000347507.3:n.2287-136_2287-135delinsCT
NM_000257.3:c.2287-136_2287-135delinsCT	NP_000248.2:n.2287-136_2287-135delinsCT
XR_245686.3:n.2393-136_2393-135delinsCT
XM_017021340.1:c.2287-136_2287-135delinsCT	XP_016876829.1:n.2287-136_2287-135delinsCT
NM_000257.4:c.2287-136_2287-135delinsCT MANE Select	NP_000248.2:n.2287-136_2287-135delinsCT