Canonical Allele Identifier: CA411382163

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36292028C>A , CM000684.2:g.36292028C>A	GRCh38
NC_000022.10:g.36688074C>A , CM000684.1:g.36688074C>A	GRCh37
NC_000022.9:g.35018020C>A	NCBI36
NG_011884.2:g.100991G>T , LRG_567:g.100991G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.4302G>T MANE Select	NP_002464.1:p.Gln1434His
ENST00000216181.11:c.4302G>T MANE Select	ENSP00000216181.6:p.Gln1434His
NM_002473.5:c.4302G>T , LRG_567t1:c.4302G>T	NP_002464.1:p.Gln1434His
ENST00000216181.9:c.4302G>T	ENSP00000216181.5:p.Gln1434His
ENST00000685801.1:c.4365G>T	ENSP00000510688.1:p.Gln1455His
ENST00000691109.1:n.4597G>T
XM_011530197.1:c.4302G>T	XP_011528499.1:p.Gln1434His
XM_011530197.2:c.4302G>T	XP_011528499.1:p.Gln1434His
XM_017028803.1:c.4302G>T	XP_016884292.1:p.Gln1434His
XM_017028804.1:c.4302G>T	XP_016884293.1:p.Gln1434His
XM_017028805.1:c.4302G>T	XP_016884294.1:p.Gln1434His
XM_017028806.1:c.4302G>T	XP_016884295.1:p.Gln1434His