Canonical Allele Identifier: CA2247333566

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639785_10639786delinsCA , CM000679.2:g.10639785_10639786delinsCA	GRCh38
NC_000017.10:g.10543102_10543103delinsCA , CM000679.1:g.10543102_10543103delinsCA	GRCh37
NC_000017.9:g.10483827_10483828delinsCA	NCBI36
NG_011537.1:g.22513_22514delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2699_2700delinsTG MANE Select	ENSP00000464317.1:p.Leu900=
ENST00000583535.5:c.2699_2700delinsTG	ENSP00000464317.1:p.Leu900=
NM_002470.3:c.2699_2700delinsTG	NP_002461.2:p.Leu900=
XM_011523870.1:c.2699_2700delinsTG	XP_011522172.1:p.Leu900=
XM_011523871.1:c.2699_2700delinsTG	XP_011522173.1:p.Leu900=
XM_011523872.1:c.2699_2700delinsTG	XP_011522174.1:p.Leu900=
XM_011523870.3:c.2699_2700delinsTG	XP_011522172.1:p.Leu900=
XM_011523871.2:c.2699_2700delinsTG	XP_011522173.1:p.Leu900=
NM_002470.4:c.2699_2700delinsTG MANE Select	NP_002461.2:p.Leu900=