Canonical Allele Identifier: CA10575521

Gene: MYH9

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36296909_36296929del , CM000684.2:g.36296909_36296929del	GRCh38
NC_000022.10:g.36692955_36692975del , CM000684.1:g.36692955_36692975del	GRCh37
NC_000022.9:g.35022901_35022921del	NCBI36
NG_011884.2:g.96099_96119del , LRG_567:g.96099_96119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685801.1:c.3258_3278del	ENSP00000510688.1:p.Glu1087_Ala1093del
ENST00000691109.1:n.3490_3510del
ENST00000216181.11:c.3195_3215del MANE Select	ENSP00000216181.6:p.Glu1066_Ala1072del
ENST00000216181.9:c.3195_3215del	ENSP00000216181.5:p.Glu1066_Ala1072del
ENST00000459960.1:n.404_424del
NM_002473.5:c.3195_3215del , LRG_567t1:c.3195_3215del	NP_002464.1:p.Glu1066_Ala1072del
XM_011530197.1:c.3195_3215del	XP_011528499.1:p.Glu1066_Ala1072del
XM_011530197.2:c.3195_3215del	XP_011528499.1:p.Glu1066_Ala1072del
XM_017028803.1:c.3195_3215del	XP_016884292.1:p.Glu1066_Ala1072del
XM_017028804.1:c.3195_3215del	XP_016884293.1:p.Glu1066_Ala1072del
XM_017028805.1:c.3195_3215del	XP_016884294.1:p.Glu1066_Ala1072del
XM_017028806.1:c.3195_3215del	XP_016884295.1:p.Glu1066_Ala1072del
NM_002473.6:c.3195_3215del MANE Select	NP_002464.1:p.Glu1066_Ala1072del