Canonical Allele Identifier: CA612937018
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1280481100

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421163_23421164del , CM000676.2:g.23421163_23421164del GRCh38
NC_000014.8:g.23890372_23890373del , CM000676.1:g.23890372_23890373del GRCh37
NC_000014.7:g.22960212_22960213del NCBI36
NG_007884.1:g.19498_19499del , LRG_384:g.19498_19499del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-116_3246-115del MANE Select ENSP00000347507.3:n.3246-116_3246-115del
ENST00000355349.3:c.3246-116_3246-115del ENSP00000347507.3:n.3246-116_3246-115del
NM_000257.3:c.3246-116_3246-115del NP_000248.2:n.3246-116_3246-115del
XR_245686.3:n.3354-116_3354-115del
XM_017021340.1:c.3246-116_3246-115del XP_016876829.1:n.3246-116_3246-115del
NM_000257.4:c.3246-116_3246-115del MANE Select NP_000248.2:n.3246-116_3246-115del