Canonical Allele Identifier: CA411387917

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36295068C>G , CM000684.2:g.36295068C>G	GRCh38
NC_000022.10:g.36691114C>G , CM000684.1:g.36691114C>G	GRCh37
NC_000022.9:g.35021060C>G	NCBI36
NG_011884.2:g.97951G>C , LRG_567:g.97951G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.3494G>C MANE Select	NP_002464.1:p.Arg1165Pro
ENST00000216181.11:c.3494G>C MANE Select	ENSP00000216181.6:p.Arg1165Pro
NM_002473.5:c.3494G>C , LRG_567t1:c.3494G>C	NP_002464.1:p.Arg1165Pro
ENST00000216181.9:c.3494G>C	ENSP00000216181.5:p.Arg1165Pro
ENST00000685801.1:c.3557G>C	ENSP00000510688.1:p.Arg1186Pro
ENST00000691109.1:n.3789G>C
XM_011530197.1:c.3494G>C	XP_011528499.1:p.Arg1165Pro
XM_011530197.2:c.3494G>C	XP_011528499.1:p.Arg1165Pro
XM_017028803.1:c.3494G>C	XP_016884292.1:p.Arg1165Pro
XM_017028804.1:c.3494G>C	XP_016884293.1:p.Arg1165Pro
XM_017028805.1:c.3494G>C	XP_016884294.1:p.Arg1165Pro
XM_017028806.1:c.3494G>C	XP_016884295.1:p.Arg1165Pro