Canonical Allele Identifier: CA411402037

Gene: MYH9

Linked Data

• MyVariant Identifiers: chr22:g.36712603A>T (hg19) ; chr22:g.36316558A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36316558A>T , CM000684.2:g.36316558A>T	GRCh38
NC_000022.10:g.36712603A>T , CM000684.1:g.36712603A>T	GRCh37
NC_000022.9:g.35042549A>T	NCBI36
NG_011884.2:g.76461T>A , LRG_567:g.76461T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.1553T>A
ENST00000685801.1:c.1339T>A	ENSP00000510688.1:p.Phe447Ile
ENST00000691109.1:n.1634T>A
ENST00000691687.1:n.2137T>A
ENST00000692930.1:n.1553T>A
ENST00000216181.11:c.1339T>A MANE Select	ENSP00000216181.6:p.Phe447Ile
ENST00000216181.9:c.1339T>A	ENSP00000216181.5:p.Phe447Ile
ENST00000477189.1:n.527T>A
NM_002473.5:c.1339T>A , LRG_567t1:c.1339T>A	NP_002464.1:p.Phe447Ile
XM_011530197.1:c.1339T>A	XP_011528499.1:p.Phe447Ile
XM_011530197.2:c.1339T>A	XP_011528499.1:p.Phe447Ile
XM_017028803.1:c.1339T>A	XP_016884292.1:p.Phe447Ile
XM_017028804.1:c.1339T>A	XP_016884293.1:p.Phe447Ile
XM_017028805.1:c.1339T>A	XP_016884294.1:p.Phe447Ile
XM_017028806.1:c.1339T>A	XP_016884295.1:p.Phe447Ile
NM_002473.6:c.1339T>A MANE Select	NP_002464.1:p.Phe447Ile