Canonical Allele Identifier: CA2636109428
Gene: MYH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639524_10639529dup , CM000679.2:g.10639524_10639529dup GRCh38
NC_000017.10:g.10542841_10542846dup , CM000679.1:g.10542841_10542846dup GRCh37
NC_000017.9:g.10483566_10483571dup NCBI36
NG_011537.1:g.22770_22775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2925+31_2925+36dup MANE Select ENSP00000464317.1:n.2925+31_2925+36dup
ENST00000583535.5:c.2925+31_2925+36dup ENSP00000464317.1:n.2925+31_2925+36dup
NM_002470.3:c.2925+31_2925+36dup NP_002461.2:n.2925+31_2925+36dup
XM_011523870.1:c.2925+31_2925+36dup XP_011522172.1:n.2925+31_2925+36dup
XM_011523871.1:c.2925+31_2925+36dup XP_011522173.1:n.2925+31_2925+36dup
XM_011523872.1:c.2925+31_2925+36dup XP_011522174.1:n.2925+31_2925+36dup
XM_011523870.3:c.2925+31_2925+36dup XP_011522172.1:n.2925+31_2925+36dup
XM_011523871.2:c.2925+31_2925+36dup XP_011522173.1:n.2925+31_2925+36dup
NM_002470.4:c.2925+31_2925+36dup MANE Select NP_002461.2:n.2925+31_2925+36dup