Canonical Allele Identifier: CA2123441853

Gene: MYH7

Linked Data

• dbSNP Id: rs1892290582

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417858_23417872del , CM000676.2:g.23417858_23417872del	GRCh38
NC_000014.8:g.23887067_23887081del , CM000676.1:g.23887067_23887081del	GRCh37
NC_000014.7:g.22956907_22956921del	NCBI36
NG_007884.1:g.22794_22808del , LRG_384:g.22794_22808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-182_4170-168del MANE Select	ENSP00000347507.3:n.4170-182_4170-168del
ENST00000355349.3:c.4170-182_4170-168del	ENSP00000347507.3:n.4170-182_4170-168del
NM_000257.3:c.4170-182_4170-168del	NP_000248.2:n.4170-182_4170-168del
XM_017021340.1:c.4170-182_4170-168del	XP_016876829.1:n.4170-182_4170-168del
NM_000257.4:c.4170-182_4170-168del MANE Select	NP_000248.2:n.4170-182_4170-168del