Canonical Allele Identifier: CA2247333062

Gene: MYH3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639473_10639474delinsAC , CM000679.2:g.10639473_10639474delinsAC	GRCh38
NC_000017.10:g.10542790_10542791delinsAC , CM000679.1:g.10542790_10542791delinsAC	GRCh37
NC_000017.9:g.10483515_10483516delinsAC	NCBI36
NG_011537.1:g.22825_22826delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2926_2927delinsGT MANE Select	ENSP00000464317.1:p.Val976=
ENST00000583535.5:c.2926_2927delinsGT	ENSP00000464317.1:p.Val976=
NM_002470.3:c.2926_2927delinsGT	NP_002461.2:p.Val976=
XM_011523870.1:c.2926_2927delinsGT	XP_011522172.1:p.Val976=
XM_011523871.1:c.2926_2927delinsGT	XP_011522173.1:p.Val976=
XM_011523872.1:c.2926_2927delinsGT	XP_011522174.1:p.Val976=
XM_011523870.3:c.2926_2927delinsGT	XP_011522172.1:p.Val976=
XM_011523871.2:c.2926_2927delinsGT	XP_011522173.1:p.Val976=
NM_002470.4:c.2926_2927delinsGT MANE Select	NP_002461.2:p.Val976=