Canonical Allele Identifier: CA725975599

Gene: MYH3

Linked Data

• dbSNP Id: rs1367723444
• MyVariant Identifiers: chr17:g.10543253_10543256del (hg19) ; chr17:g.10639936_10639939del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639936_10639939del , CM000679.2:g.10639936_10639939del	GRCh38
NC_000017.10:g.10543253_10543256del , CM000679.1:g.10543253_10543256del	GRCh37
NC_000017.9:g.10483978_10483981del	NCBI36
NG_011537.1:g.22360_22363del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2682+57_2682+60del MANE Select	ENSP00000464317.1:n.2682+57_2682+60del
ENST00000583535.5:c.2682+57_2682+60del	ENSP00000464317.1:n.2682+57_2682+60del
NM_002470.3:c.2682+57_2682+60del	NP_002461.2:n.2682+57_2682+60del
XM_011523870.1:c.2682+57_2682+60del	XP_011522172.1:n.2682+57_2682+60del
XM_011523871.1:c.2682+57_2682+60del	XP_011522173.1:n.2682+57_2682+60del
XM_011523872.1:c.2682+57_2682+60del	XP_011522174.1:n.2682+57_2682+60del
XM_011523870.3:c.2682+57_2682+60del	XP_011522172.1:n.2682+57_2682+60del
XM_011523871.2:c.2682+57_2682+60del	XP_011522173.1:n.2682+57_2682+60del
NM_002470.4:c.2682+57_2682+60del MANE Select	NP_002461.2:n.2682+57_2682+60del