Canonical Allele Identifier: CA2247333084

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639484_10639485delinsAT , CM000679.2:g.10639484_10639485delinsAT	GRCh38
NC_000017.10:g.10542801_10542802delinsAT , CM000679.1:g.10542801_10542802delinsAT	GRCh37
NC_000017.9:g.10483526_10483527delinsAT	NCBI36
NG_011537.1:g.22814_22815delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2926-11_2926-10delinsAT MANE Select	ENSP00000464317.1:n.2926-11_2926-10delinsAT
ENST00000583535.5:c.2926-11_2926-10delinsAT	ENSP00000464317.1:n.2926-11_2926-10delinsAT
NM_002470.3:c.2926-11_2926-10delinsAT	NP_002461.2:n.2926-11_2926-10delinsAT
XM_011523870.1:c.2926-11_2926-10delinsAT	XP_011522172.1:n.2926-11_2926-10delinsAT
XM_011523871.1:c.2926-11_2926-10delinsAT	XP_011522173.1:n.2926-11_2926-10delinsAT
XM_011523872.1:c.2926-11_2926-10delinsAT	XP_011522174.1:n.2926-11_2926-10delinsAT
XM_011523870.3:c.2926-11_2926-10delinsAT	XP_011522172.1:n.2926-11_2926-10delinsAT
XM_011523871.2:c.2926-11_2926-10delinsAT	XP_011522173.1:n.2926-11_2926-10delinsAT
NM_002470.4:c.2926-11_2926-10delinsAT MANE Select	NP_002461.2:n.2926-11_2926-10delinsAT