Canonical Allele Identifier: CA613318002
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1176284834

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417686_23417687insTTGGCCTCCTCGAGCTCCTCAGTCCG , CM000676.2:g.23417686_23417687insTTGGCCTCCTCGAGCTCCTCAGTCCG GRCh38
NC_000014.8:g.23886895_23886896insTTGGCCTCCTCGAGCTCCTCAGTCCG , CM000676.1:g.23886895_23886896insTTGGCCTCCTCGAGCTCCTCAGTCCG GRCh37
NC_000014.7:g.22956735_22956736insTTGGCCTCCTCGAGCTCCTCAGTCCG NCBI36
NG_007884.1:g.22975_22976insCGGACTGAGGAGCTCGAGGAGGCCAA , LRG_384:g.22975_22976insCGGACTGAGGAGCTCGAGGAGGCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA MANE Select ENSP00000347507.3:n.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA
ENST00000355349.3:c.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA ENSP00000347507.3:n.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA
NM_000257.3:c.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA NP_000248.2:n.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA
XM_017021340.1:c.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA XP_016876829.1:n.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA
NM_000257.4:c.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA MANE Select NP_000248.2:n.4170-1_4170insCGGACTGAGGAGCTCGAGGAGGCCAA