Canonical Allele Identifier: CA2636109390

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639460-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639461del , CM000679.2:g.10639461del	GRCh38
NC_000017.10:g.10542778del , CM000679.1:g.10542778del	GRCh37
NC_000017.9:g.10483503del	NCBI36
NG_011537.1:g.22838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2939del MANE Select	ENSP00000464317.1:p.Thr980MetfsTer7
ENST00000583535.5:c.2939del	ENSP00000464317.1:p.Thr980MetfsTer7
NM_002470.3:c.2939del	NP_002461.2:p.Thr980MetfsTer7
XM_011523870.1:c.2939del	XP_011522172.1:p.Thr980MetfsTer7
XM_011523871.1:c.2939del	XP_011522173.1:p.Thr980MetfsTer7
XM_011523872.1:c.2939del	XP_011522174.1:p.Thr980MetfsTer7
XM_011523870.3:c.2939del	XP_011522172.1:p.Thr980MetfsTer7
XM_011523871.2:c.2939del	XP_011522173.1:p.Thr980MetfsTer7
NM_002470.4:c.2939del MANE Select	NP_002461.2:p.Thr980MetfsTer7