Canonical Allele Identifier: CA2636109449
Gene: MYH3 HGNC NCBI

Linked Data

gnomAD v4: 17-10639569-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639570del , CM000679.2:g.10639570del GRCh38
NC_000017.10:g.10542887del , CM000679.1:g.10542887del GRCh37
NC_000017.9:g.10483612del NCBI36
NG_011537.1:g.22729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2915del MANE Select ENSP00000464317.1:p.Thr972LysfsTer15
ENST00000583535.5:c.2915del ENSP00000464317.1:p.Thr972LysfsTer15
NM_002470.3:c.2915del NP_002461.2:p.Thr972LysfsTer15
XM_011523870.1:c.2915del XP_011522172.1:p.Thr972LysfsTer15
XM_011523871.1:c.2915del XP_011522173.1:p.Thr972LysfsTer15
XM_011523872.1:c.2915del XP_011522174.1:p.Thr972LysfsTer15
XM_011523870.3:c.2915del XP_011522172.1:p.Thr972LysfsTer15
XM_011523871.2:c.2915del XP_011522173.1:p.Thr972LysfsTer15
NM_002470.4:c.2915del MANE Select NP_002461.2:p.Thr972LysfsTer15
Search 100 bp 5'
Search 100 bp 3'