Canonical Allele Identifier: CA2636109478

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639791-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639795del , CM000679.2:g.10639795del	GRCh38
NC_000017.10:g.10543112del , CM000679.1:g.10543112del	GRCh37
NC_000017.9:g.10483837del	NCBI36
NG_011537.1:g.22507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2693del MANE Select	ENSP00000464317.1:p.Asn898IlefsTer12
ENST00000583535.5:c.2693del	ENSP00000464317.1:p.Asn898IlefsTer12
NM_002470.3:c.2693del	NP_002461.2:p.Asn898IlefsTer12
XM_011523870.1:c.2693del	XP_011522172.1:p.Asn898IlefsTer12
XM_011523871.1:c.2693del	XP_011522173.1:p.Asn898IlefsTer12
XM_011523872.1:c.2693del	XP_011522174.1:p.Asn898IlefsTer12
XM_011523870.3:c.2693del	XP_011522172.1:p.Asn898IlefsTer12
XM_011523871.2:c.2693del	XP_011522173.1:p.Asn898IlefsTer12
NM_002470.4:c.2693del MANE Select	NP_002461.2:p.Asn898IlefsTer12