Canonical Allele Identifier: CA2123457993

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425608_23425609delinsTG , CM000676.2:g.23425608_23425609delinsTG	GRCh38
NC_000014.8:g.23894817_23894818delinsTG , CM000676.1:g.23894817_23894818delinsTG	GRCh37
NC_000014.7:g.22964657_22964658delinsTG	NCBI36
NG_007884.1:g.15053_15054delinsCA , LRG_384:g.15053_15054delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2286+86_2286+87delinsCA MANE Select	ENSP00000347507.3:n.2286+86_2286+87delinsCA
ENST00000355349.3:c.2286+86_2286+87delinsCA	ENSP00000347507.3:n.2286+86_2286+87delinsCA
NM_000257.3:c.2286+86_2286+87delinsCA	NP_000248.2:n.2286+86_2286+87delinsCA
XR_245686.3:n.2392+86_2392+87delinsCA
XM_017021340.1:c.2286+86_2286+87delinsCA	XP_016876829.1:n.2286+86_2286+87delinsCA
NM_000257.4:c.2286+86_2286+87delinsCA MANE Select	NP_000248.2:n.2286+86_2286+87delinsCA