Canonical Allele Identifier: CA920364526

Gene: MYH9

Linked Data

• dbSNP Id: rs1603482634

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36281827_36281828dup , CM000684.2:g.36281827_36281828dup	GRCh38
NC_000022.10:g.36677873_36677874dup , CM000684.1:g.36677873_36677874dup	GRCh37
NC_000022.9:g.35007819_35007820dup	NCBI36
NG_011884.2:g.111192_111193dup , LRG_567:g.111192_111193dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.3157_3158dup
ENST00000685801.1:c.*841_*842dup	ENSP00000510688.1:n.*841_*842dup
ENST00000690244.1:n.2060_2061dup
ENST00000691109.1:n.7019_7020dup
ENST00000216181.11:c.*841_*842dup MANE Select	ENSP00000216181.6:n.*841_*842dup
ENST00000216181.9:c.*841_*842dup	ENSP00000216181.5:n.*841_*842dup
NM_002473.5:c.*841_*842dup , LRG_567t1:c.*841_*842dup	NP_002464.1:n.*841_*842dup
XM_011530197.1:c.*841_*842dup	XP_011528499.1:n.*841_*842dup
XM_011530197.2:c.*841_*842dup	XP_011528499.1:n.*841_*842dup
XM_017028803.1:c.*841_*842dup	XP_016884292.1:n.*841_*842dup
XM_017028804.1:c.*841_*842dup	XP_016884293.1:n.*841_*842dup
XM_017028805.1:c.*841_*842dup	XP_016884294.1:n.*841_*842dup
XM_017028806.1:c.*841_*842dup	XP_016884295.1:n.*841_*842dup
NM_002473.6:c.*841_*842dup MANE Select	NP_002464.1:n.*841_*842dup