Canonical Allele Identifier: CA2123441539

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417701_23417702delinsGT , CM000676.2:g.23417701_23417702delinsGT	GRCh38
NC_000014.8:g.23886910_23886911delinsGT , CM000676.1:g.23886910_23886911delinsGT	GRCh37
NC_000014.7:g.22956750_22956751delinsGT	NCBI36
NG_007884.1:g.22960_22961delinsAC , LRG_384:g.22960_22961delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-16_4170-15delinsAC MANE Select	ENSP00000347507.3:n.4170-16_4170-15delinsAC
ENST00000355349.3:c.4170-16_4170-15delinsAC	ENSP00000347507.3:n.4170-16_4170-15delinsAC
NM_000257.3:c.4170-16_4170-15delinsAC	NP_000248.2:n.4170-16_4170-15delinsAC
XM_017021340.1:c.4170-16_4170-15delinsAC	XP_016876829.1:n.4170-16_4170-15delinsAC
NM_000257.4:c.4170-16_4170-15delinsAC MANE Select	NP_000248.2:n.4170-16_4170-15delinsAC