Canonical Allele Identifier: CA2247317242

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639956_10639957delinsAG , CM000679.2:g.10639956_10639957delinsAG	GRCh38
NC_000017.10:g.10543273_10543274delinsAG , CM000679.1:g.10543273_10543274delinsAG	GRCh37
NC_000017.9:g.10483998_10483999delinsAG	NCBI36
NG_011537.1:g.22342_22343delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000583535.6:c.2682+39_2682+40delinsCT MANE Select	ENSP00000464317.1:n.2682+39_2682+40delins...
ENST00000583535.5:c.2682+39_2682+40delinsCT	ENSP00000464317.1:n.2682+39_2682+40delins...
NM_002470.3:c.2682+39_2682+40delinsCT	NP_002461.2:n.2682+39_2682+40delinsCT
XM_011523870.1:c.2682+39_2682+40delinsCT	XP_011522172.1:n.2682+39_2682+40delinsCT
XM_011523871.1:c.2682+39_2682+40delinsCT	XP_011522173.1:n.2682+39_2682+40delinsCT
XM_011523872.1:c.2682+39_2682+40delinsCT	XP_011522174.1:n.2682+39_2682+40delinsCT
XM_011523870.3:c.2682+39_2682+40delinsCT	XP_011522172.1:n.2682+39_2682+40delinsCT
XM_011523871.2:c.2682+39_2682+40delinsCT	XP_011522173.1:n.2682+39_2682+40delinsCT
NM_002470.4:c.2682+39_2682+40delinsCT MANE Select	NP_002461.2:n.2682+39_2682+40delinsCT