Canonical Allele Identifier: CA2800863526
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424321_23424322insAGTT , CM000676.2:g.23424321_23424322insAGTT GRCh38
NC_000014.8:g.23893530_23893531insAGTT , CM000676.1:g.23893530_23893531insAGTT GRCh37
NC_000014.7:g.22963370_22963371insAGTT NCBI36
NG_007884.1:g.16340_16341insAACT , LRG_384:g.16340_16341insAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-173_2680-172insAACT MANE Select ENSP00000347507.3:n.2680-173_2680-172insAACT
ENST00000355349.3:c.2680-173_2680-172insAACT ENSP00000347507.3:n.2680-173_2680-172insAACT
NM_000257.3:c.2680-173_2680-172insAACT NP_000248.2:n.2680-173_2680-172insAACT
XR_245686.3:n.2786-173_2786-172insAACT
XM_017021340.1:c.2680-173_2680-172insAACT XP_016876829.1:n.2680-173_2680-172insAACT
NM_000257.4:c.2680-173_2680-172insAACT MANE Select NP_000248.2:n.2680-173_2680-172insAACT