Canonical Allele Identifier: CA2123451820

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431510_23431511delinsGT , CM000676.2:g.23431510_23431511delinsGT	GRCh38
NC_000014.8:g.23900719_23900720delinsGT , CM000676.1:g.23900719_23900720delinsGT	GRCh37
NC_000014.7:g.22970559_22970560delinsGT	NCBI36
NG_007884.1:g.9151_9152delinsAC , LRG_384:g.9151_9152delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.733-30_733-29delinsAC MANE Select	ENSP00000347507.3:n.733-30_733-29delinsAC
ENST00000355349.3:c.733-30_733-29delinsAC	ENSP00000347507.3:n.733-30_733-29delinsAC
NM_000257.3:c.733-30_733-29delinsAC	NP_000248.2:n.733-30_733-29delinsAC
XR_245686.3:n.839-30_839-29delinsAC
XM_017021340.1:c.733-30_733-29delinsAC	XP_016876829.1:n.733-30_733-29delinsAC
NM_000257.4:c.733-30_733-29delinsAC MANE Select	NP_000248.2:n.733-30_733-29delinsAC