Canonical Allele Identifier: CA2403798190

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36288308T= , CM000684.2:g.36288308T=	GRCh38
NC_000022.10:g.36684354T= , CM000684.1:g.36684354T=	GRCh37
NC_000022.9:g.35014300T=	NCBI36
NG_011884.2:g.104711A= , LRG_567:g.104711A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.4876A= MANE Select	NP_002464.1:p.Ile1626=
ENST00000216181.11:c.4876A= MANE Select	ENSP00000216181.6:p.Ile1626=
NM_002473.5:c.4876A= , LRG_567t1:c.4876A=	NP_002464.1:p.Ile1626=
ENST00000216181.9:c.4876A=	ENSP00000216181.5:p.Ile1626=
ENST00000685801.1:c.4939A=	ENSP00000510688.1:p.Ile1647=
ENST00000691109.1:n.5171A=
XM_011530197.1:c.4876A=	XP_011528499.1:p.Ile1626=
XM_011530197.2:c.4876A=	XP_011528499.1:p.Ile1626=
XM_017028803.1:c.4876A=	XP_016884292.1:p.Ile1626=
XM_017028804.1:c.4876A=	XP_016884293.1:p.Ile1626=
XM_017028805.1:c.4876A=	XP_016884294.1:p.Ile1626=
XM_017028806.1:c.4876A=	XP_016884295.1:p.Ile1626=