Canonical Allele Identifier: CA2576173406

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639949-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639951_10639952del , CM000679.2:g.10639951_10639952del	GRCh38
NC_000017.10:g.10543268_10543269del , CM000679.1:g.10543268_10543269del	GRCh37
NC_000017.9:g.10483993_10483994del	NCBI36
NG_011537.1:g.22348_22349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2682+45_2682+46del MANE Select	ENSP00000464317.1:n.2682+45_2682+46del
ENST00000583535.5:c.2682+45_2682+46del	ENSP00000464317.1:n.2682+45_2682+46del
NM_002470.3:c.2682+45_2682+46del	NP_002461.2:n.2682+45_2682+46del
XM_011523870.1:c.2682+45_2682+46del	XP_011522172.1:n.2682+45_2682+46del
XM_011523871.1:c.2682+45_2682+46del	XP_011522173.1:n.2682+45_2682+46del
XM_011523872.1:c.2682+45_2682+46del	XP_011522174.1:n.2682+45_2682+46del
XM_011523870.3:c.2682+45_2682+46del	XP_011522172.1:n.2682+45_2682+46del
XM_011523871.2:c.2682+45_2682+46del	XP_011522173.1:n.2682+45_2682+46del
NM_002470.4:c.2682+45_2682+46del MANE Select	NP_002461.2:n.2682+45_2682+46del