Canonical Allele Identifier: CA2636109633

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639964-T-TAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639976_10639978dup , CM000679.2:g.10639976_10639978dup	GRCh38
NC_000017.10:g.10543293_10543295dup , CM000679.1:g.10543293_10543295dup	GRCh37
NC_000017.9:g.10484018_10484020dup	NCBI36
NG_011537.1:g.22332_22334dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000583535.6:c.2682+29_2682+31dup MANE Select	ENSP00000464317.1:n.2682+29_2682+31dup
ENST00000583535.5:c.2682+29_2682+31dup	ENSP00000464317.1:n.2682+29_2682+31dup
NM_002470.3:c.2682+29_2682+31dup	NP_002461.2:n.2682+29_2682+31dup
XM_011523870.1:c.2682+29_2682+31dup	XP_011522172.1:n.2682+29_2682+31dup
XM_011523871.1:c.2682+29_2682+31dup	XP_011522173.1:n.2682+29_2682+31dup
XM_011523872.1:c.2682+29_2682+31dup	XP_011522174.1:n.2682+29_2682+31dup
XM_011523870.3:c.2682+29_2682+31dup	XP_011522172.1:n.2682+29_2682+31dup
XM_011523871.2:c.2682+29_2682+31dup	XP_011522173.1:n.2682+29_2682+31dup
NM_002470.4:c.2682+29_2682+31dup MANE Select	NP_002461.2:n.2682+29_2682+31dup