Canonical Allele Identifier: CA10210206

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36309401C>T , CM000684.2:g.36309401C>T	GRCh38
NC_000022.10:g.36705446C>T , CM000684.1:g.36705446C>T	GRCh37
NC_000022.9:g.35035392C>T	NCBI36
NG_011884.2:g.83618G>A , LRG_567:g.83618G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.1729-5G>A MANE Select	NP_002464.1:n.1729-5G>A
ENST00000216181.11:c.1729-5G>A MANE Select	ENSP00000216181.6:n.1729-5G>A
NM_002473.5:c.1729-5G>A , LRG_567t1:c.1729-5G>A	NP_002464.1:n.1729-5G>A
ENST00000216181.9:c.1729-5G>A	ENSP00000216181.5:n.1729-5G>A
ENST00000685801.1:c.1729-5G>A	ENSP00000510688.1:n.1729-5G>A
ENST00000687922.1:n.60G>A
ENST00000691109.1:n.2024-5G>A
ENST00000692930.1:n.1943-5G>A
XM_011530197.1:c.1729-5G>A	XP_011528499.1:n.1729-5G>A
XM_011530197.2:c.1729-5G>A	XP_011528499.1:n.1729-5G>A
XM_017028803.1:c.1729-5G>A	XP_016884292.1:n.1729-5G>A
XM_017028804.1:c.1729-5G>A	XP_016884293.1:n.1729-5G>A
XM_017028805.1:c.1729-5G>A	XP_016884294.1:n.1729-5G>A
XM_017028806.1:c.1729-5G>A	XP_016884295.1:n.1729-5G>A