Canonical Allele Identifier: CA10575522

Gene: MYH9

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36296909_36296929dup , CM000684.2:g.36296909_36296929dup	GRCh38
NC_000022.10:g.36692955_36692975dup , CM000684.1:g.36692955_36692975dup	GRCh37
NC_000022.9:g.35022901_35022921dup	NCBI36
NG_011884.2:g.96099_96119dup , LRG_567:g.96099_96119dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685801.1:c.3258_3278dup	ENSP00000510688.1:p.Ala1093_Glu1094insGluLeuGlnAlaGlnIleAla
ENST00000691109.1:n.3490_3510dup
ENST00000216181.11:c.3195_3215dup MANE Select	ENSP00000216181.6:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
ENST00000216181.9:c.3195_3215dup	ENSP00000216181.5:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
ENST00000459960.1:n.404_424dup
NM_002473.5:c.3195_3215dup , LRG_567t1:c.3195_3215dup	NP_002464.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
XM_011530197.1:c.3195_3215dup	XP_011528499.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
XM_011530197.2:c.3195_3215dup	XP_011528499.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
XM_017028803.1:c.3195_3215dup	XP_016884292.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
XM_017028804.1:c.3195_3215dup	XP_016884293.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
XM_017028805.1:c.3195_3215dup	XP_016884294.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
XM_017028806.1:c.3195_3215dup	XP_016884295.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla
NM_002473.6:c.3195_3215dup MANE Select	NP_002464.1:p.Ala1072_Glu1073insGluLeuGlnAlaGlnIleAla