Canonical Allele Identifier: CA2247333135

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639503_10639510delinsCTTAAAGT , CM000679.2:g.10639503_10639510delinsCTTAAAGT	GRCh38
NC_000017.10:g.10542820_10542827delinsCTTAAAGT , CM000679.1:g.10542820_10542827delinsCTTAAAGT	GRCh37
NC_000017.9:g.10483545_10483552delinsCTTAAAGT	NCBI36
NG_011537.1:g.22789_22796delinsACTTTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2926-36_2926-29delinsACTTTAAG MANE Select	ENSP00000464317.1:n.2926-36_2926-29delinsACTTTAAG
ENST00000583535.5:c.2926-36_2926-29delinsACTTTAAG	ENSP00000464317.1:n.2926-36_2926-29delinsACTTTAAG
NM_002470.3:c.2926-36_2926-29delinsACTTTAAG	NP_002461.2:n.2926-36_2926-29delinsACTTTAAG
XM_011523870.1:c.2926-36_2926-29delinsACTTTAAG	XP_011522172.1:n.2926-36_2926-29delinsACTTTAAG
XM_011523871.1:c.2926-36_2926-29delinsACTTTAAG	XP_011522173.1:n.2926-36_2926-29delinsACTTTAAG
XM_011523872.1:c.2926-36_2926-29delinsACTTTAAG	XP_011522174.1:n.2926-36_2926-29delinsACTTTAAG
XM_011523870.3:c.2926-36_2926-29delinsACTTTAAG	XP_011522172.1:n.2926-36_2926-29delinsACTTTAAG
XM_011523871.2:c.2926-36_2926-29delinsACTTTAAG	XP_011522173.1:n.2926-36_2926-29delinsACTTTAAG
NM_002470.4:c.2926-36_2926-29delinsACTTTAAG MANE Select	NP_002461.2:n.2926-36_2926-29delinsACTTTAAG