Canonical Allele Identifier: CA2123455002
Gene: MYH7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424296_23424298delinsAAG , CM000676.2:g.23424296_23424298delinsAAG GRCh38
NC_000014.8:g.23893505_23893507delinsAAG , CM000676.1:g.23893505_23893507delinsAAG GRCh37
NC_000014.7:g.22963345_22963347delinsAAG NCBI36
NG_007884.1:g.16364_16366delinsCTT , LRG_384:g.16364_16366delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-149_2680-147delinsCTT MANE Select ENSP00000347507.3:n.2680-149_2680-147delinsCTT
ENST00000355349.3:c.2680-149_2680-147delinsCTT ENSP00000347507.3:n.2680-149_2680-147delinsCTT
NM_000257.3:c.2680-149_2680-147delinsCTT NP_000248.2:n.2680-149_2680-147delinsCTT
XR_245686.3:n.2786-149_2786-147delinsCTT
XM_017021340.1:c.2680-149_2680-147delinsCTT XP_016876829.1:n.2680-149_2680-147delinsCTT
NM_000257.4:c.2680-149_2680-147delinsCTT MANE Select NP_000248.2:n.2680-149_2680-147delinsCTT
Search 100 bp 5'
Search 100 bp 3'