Canonical Allele Identifier: CA2624251931
Gene: MYH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23393604_23393605del , CM000676.2:g.23393604_23393605del GRCh38
NC_000014.8:g.23862813_23862814del , CM000676.1:g.23862813_23862814del GRCh37
NC_000014.7:g.22932653_22932654del NCBI36
NG_023444.1:g.19674_19675del , LRG_389:g.19674_19675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405093.9:c.2928+62_2928+63del MANE Select ENSP00000386041.3:n.2928+62_2928+63del
ENST00000356287.3:c.2928+62_2928+63del ENSP00000348634.3:n.2928+62_2928+63del
ENST00000405093.7:c.2928+62_2928+63del ENSP00000386041.3:n.2928+62_2928+63del
NM_002471.3:c.2928+62_2928+63del , LRG_389t1:c.2928+62_2928+63del NP_002462.2:n.2928+62_2928+63del
NM_002471.4:c.2928+62_2928+63del MANE Select NP_002462.2:n.2928+62_2928+63del