Canonical Allele Identifier: CA2123413463
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23392874_23392875delinsAC , CM000676.2:g.23392874_23392875delinsAC GRCh38
NC_000014.8:g.23862083_23862084delinsAC , CM000676.1:g.23862083_23862084delinsAC GRCh37
NC_000014.7:g.22931923_22931924delinsAC NCBI36
NG_023444.1:g.20403_20404delinsGT , LRG_389:g.20403_20404delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.3251+37_3251+38delinsGT MANE Select ENSP00000386041.3:n.3251+37_3251+38delins...
ENST00000356287.3:c.3251+37_3251+38delinsGT ENSP00000348634.3:n.3251+37_3251+38delins...
ENST00000405093.7:c.3251+37_3251+38delinsGT ENSP00000386041.3:n.3251+37_3251+38delins...
NM_002471.3:c.3251+37_3251+38delinsGT , LRG_389t1:c.3251+37_3251+38delinsGT NP_002462.2:n.3251+37_3251+38delinsGT
NM_002471.4:c.3251+37_3251+38delinsGT MANE Select NP_002462.2:n.3251+37_3251+38delinsGT