Canonical Allele Identifier: CA2403801761
Community Standard Title: NM_002473.6(MYH9):c.3464C= (p.Thr1155=)
Gene: MYH9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36295526G= , CM000684.2:g.36295526G= GRCh38
NC_000022.10:g.36691572G= , CM000684.1:g.36691572G= GRCh37
NC_000022.9:g.35021518G= NCBI36
NG_011884.2:g.97493C= , LRG_567:g.97493C=

Transcript Alleles

HGVS Amino-acid Change
NM_002473.6:c.3464C= MANE Select NP_002464.1:p.Thr1155=
ENST00000216181.11:c.3464C= MANE Select ENSP00000216181.6:p.Thr1155=
NM_002473.5:c.3464C= , LRG_567t1:c.3464C= NP_002464.1:p.Thr1155=
ENST00000216181.9:c.3464C= ENSP00000216181.5:p.Thr1155=
ENST00000459960.1:n.673C=
ENST00000685801.1:c.3527C= ENSP00000510688.1:p.Thr1176=
ENST00000691109.1:n.3759C=
XM_011530197.1:c.3464C= XP_011528499.1:p.Thr1155=
XM_011530197.2:c.3464C= XP_011528499.1:p.Thr1155=
XM_017028803.1:c.3464C= XP_016884292.1:p.Thr1155=
XM_017028804.1:c.3464C= XP_016884293.1:p.Thr1155=
XM_017028805.1:c.3464C= XP_016884294.1:p.Thr1155=
XM_017028806.1:c.3464C= XP_016884295.1:p.Thr1155=