Canonical Allele Identifier: CA2123455019
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424317_23424319delinsCTT , CM000676.2:g.23424317_23424319delinsCTT GRCh38
NC_000014.8:g.23893526_23893528delinsCTT , CM000676.1:g.23893526_23893528delinsCTT GRCh37
NC_000014.7:g.22963366_22963368delinsCTT NCBI36
NG_007884.1:g.16343_16345delinsAAG , LRG_384:g.16343_16345delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-170_2680-168delinsAAG MANE Select ENSP00000347507.3:n.2680-170_2680-168delinsAAG
ENST00000355349.3:c.2680-170_2680-168delinsAAG ENSP00000347507.3:n.2680-170_2680-168delinsAAG
NM_000257.3:c.2680-170_2680-168delinsAAG NP_000248.2:n.2680-170_2680-168delinsAAG
XR_245686.3:n.2786-170_2786-168delinsAAG
XM_017021340.1:c.2680-170_2680-168delinsAAG XP_016876829.1:n.2680-170_2680-168delinsAAG
NM_000257.4:c.2680-170_2680-168delinsAAG MANE Select NP_000248.2:n.2680-170_2680-168delinsAAG
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