Canonical Allele Identifier: CA2123451797
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431496_23431497delinsGA , CM000676.2:g.23431496_23431497delinsGA GRCh38
NC_000014.8:g.23900705_23900706delinsGA , CM000676.1:g.23900705_23900706delinsGA GRCh37
NC_000014.7:g.22970545_22970546delinsGA NCBI36
NG_007884.1:g.9165_9166delinsTC , LRG_384:g.9165_9166delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.733-16_733-15delinsTC MANE Select ENSP00000347507.3:n.733-16_733-15delinsTC...
ENST00000355349.3:c.733-16_733-15delinsTC ENSP00000347507.3:n.733-16_733-15delinsTC...
NM_000257.3:c.733-16_733-15delinsTC NP_000248.2:n.733-16_733-15delinsTC
XR_245686.3:n.839-16_839-15delinsTC
XM_017021340.1:c.733-16_733-15delinsTC XP_016876829.1:n.733-16_733-15delinsTC
NM_000257.4:c.733-16_733-15delinsTC MANE Select NP_000248.2:n.733-16_733-15delinsTC