Canonical Allele Identifier: CA981429991

Gene: MYH3

Linked Data

• dbSNP Id: rs2074253058
• gnomAD v3: 17-10639937-TAAA-T
• gnomAD v4: 17-10639937-TAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639938_10639940del , CM000679.2:g.10639938_10639940del	GRCh38
NC_000017.10:g.10543255_10543257del , CM000679.1:g.10543255_10543257del	GRCh37
NC_000017.9:g.10483980_10483982del	NCBI36
NG_011537.1:g.22359_22361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2682+56_2682+58del MANE Select	ENSP00000464317.1:n.2682+56_2682+58del
ENST00000583535.5:c.2682+56_2682+58del	ENSP00000464317.1:n.2682+56_2682+58del
NM_002470.3:c.2682+56_2682+58del	NP_002461.2:n.2682+56_2682+58del
XM_011523870.1:c.2682+56_2682+58del	XP_011522172.1:n.2682+56_2682+58del
XM_011523871.1:c.2682+56_2682+58del	XP_011522173.1:n.2682+56_2682+58del
XM_011523872.1:c.2682+56_2682+58del	XP_011522174.1:n.2682+56_2682+58del
XM_011523870.3:c.2682+56_2682+58del	XP_011522172.1:n.2682+56_2682+58del
XM_011523871.2:c.2682+56_2682+58del	XP_011522173.1:n.2682+56_2682+58del
NM_002470.4:c.2682+56_2682+58del MANE Select	NP_002461.2:n.2682+56_2682+58del