Canonical Allele Identifier: CA411374571

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36286816C>T , CM000684.2:g.36286816C>T	GRCh38
NC_000022.10:g.36682862C>T , CM000684.1:g.36682862C>T	GRCh37
NC_000022.9:g.35012808C>T	NCBI36
NG_011884.2:g.106203G>A , LRG_567:g.106203G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.4963G>A MANE Select	NP_002464.1:p.Asp1655Asn
ENST00000216181.11:c.4963G>A MANE Select	ENSP00000216181.6:p.Asp1655Asn
NM_002473.5:c.4963G>A , LRG_567t1:c.4963G>A	NP_002464.1:p.Asp1655Asn
ENST00000216181.9:c.4963G>A	ENSP00000216181.5:p.Asp1655Asn
ENST00000685708.1:n.1396G>A
ENST00000685801.1:c.5026G>A	ENSP00000510688.1:p.Asp1676Asn
ENST00000691109.1:n.5258G>A
XM_011530197.1:c.4963G>A	XP_011528499.1:p.Asp1655Asn
XM_011530197.2:c.4963G>A	XP_011528499.1:p.Asp1655Asn
XM_017028803.1:c.4963G>A	XP_016884292.1:p.Asp1655Asn
XM_017028804.1:c.4963G>A	XP_016884293.1:p.Asp1655Asn
XM_017028805.1:c.4963G>A	XP_016884294.1:p.Asp1655Asn
XM_017028806.1:c.4963G>A	XP_016884295.1:p.Asp1655Asn