Canonical Allele Identifier: CA2636109485

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639805-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639814_10639815dup , CM000679.2:g.10639814_10639815dup	GRCh38
NC_000017.10:g.10543131_10543132dup , CM000679.1:g.10543131_10543132dup	GRCh37
NC_000017.9:g.10483856_10483857dup	NCBI36
NG_011537.1:g.22492_22493dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2683-5_2683-4dup MANE Select	ENSP00000464317.1:n.2683-5_2683-4dup
ENST00000583535.5:c.2683-5_2683-4dup	ENSP00000464317.1:n.2683-5_2683-4dup
NM_002470.3:c.2683-5_2683-4dup	NP_002461.2:n.2683-5_2683-4dup
XM_011523870.1:c.2683-5_2683-4dup	XP_011522172.1:n.2683-5_2683-4dup
XM_011523871.1:c.2683-5_2683-4dup	XP_011522173.1:n.2683-5_2683-4dup
XM_011523872.1:c.2683-5_2683-4dup	XP_011522174.1:n.2683-5_2683-4dup
XM_011523870.3:c.2683-5_2683-4dup	XP_011522172.1:n.2683-5_2683-4dup
XM_011523871.2:c.2683-5_2683-4dup	XP_011522173.1:n.2683-5_2683-4dup
NM_002470.4:c.2683-5_2683-4dup MANE Select	NP_002461.2:n.2683-5_2683-4dup