Canonical Allele Identifier: CA2728939110

Gene: MYH7

Linked Data

• dbSNP Id: rs1352106557

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420149dup , CM000676.2:g.23420149dup	GRCh38
NC_000014.8:g.23889358dup , CM000676.1:g.23889358dup	GRCh37
NC_000014.7:g.22959198dup	NCBI36
NG_007884.1:g.20515dup , LRG_384:g.20515dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3424dup MANE Select	ENSP00000347507.3:p.Glu1142GlyfsTer?
ENST00000355349.3:c.3424dup	ENSP00000347507.3:p.Glu1142GlyfsTer?
NM_000257.3:c.3424dup	NP_000248.2:p.Glu1142GlyfsTer?
XM_017021340.1:c.3424dup	XP_016876829.1:p.Glu1142GlyfsTer?
NM_000257.4:c.3424dup MANE Select	NP_000248.2:p.Glu1142GlyfsTer?