Canonical Allele Identifier: CA2247317254
Gene: MYH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639964_10639968delinsTAAAA , CM000679.2:g.10639964_10639968delinsTAAAA GRCh38
NC_000017.10:g.10543281_10543285delinsTAAAA , CM000679.1:g.10543281_10543285delinsTAAAA GRCh37
NC_000017.9:g.10484006_10484010delinsTAAAA NCBI36
NG_011537.1:g.22331_22335delinsTTTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000583535.6:c.2682+28_2682+32delinsTTTTA MANE Select ENSP00000464317.1:n.2682+28_2682+32delins...
ENST00000583535.5:c.2682+28_2682+32delinsTTTTA ENSP00000464317.1:n.2682+28_2682+32delins...
NM_002470.3:c.2682+28_2682+32delinsTTTTA NP_002461.2:n.2682+28_2682+32delinsTTTTA
XM_011523870.1:c.2682+28_2682+32delinsTTTTA XP_011522172.1:n.2682+28_2682+32delinsTTT...
XM_011523871.1:c.2682+28_2682+32delinsTTTTA XP_011522173.1:n.2682+28_2682+32delinsTTT...
XM_011523872.1:c.2682+28_2682+32delinsTTTTA XP_011522174.1:n.2682+28_2682+32delinsTTT...
XM_011523870.3:c.2682+28_2682+32delinsTTTTA XP_011522172.1:n.2682+28_2682+32delinsTTT...
XM_011523871.2:c.2682+28_2682+32delinsTTTTA XP_011522173.1:n.2682+28_2682+32delinsTTT...
NM_002470.4:c.2682+28_2682+32delinsTTTTA MANE Select NP_002461.2:n.2682+28_2682+32delinsTTTTA
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