Canonical Allele Identifier: CA411549551

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36349140A>C , CM000684.2:g.36349140A>C	GRCh38
NC_000022.10:g.36745185A>C , CM000684.1:g.36745185A>C	GRCh37
NC_000022.9:g.35075131A>C	NCBI36
NG_011884.2:g.43879T>G , LRG_567:g.43879T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.97T>G MANE Select	NP_002464.1:p.Trp33Gly
ENST00000216181.11:c.97T>G MANE Select	ENSP00000216181.6:p.Trp33Gly
NM_002473.5:c.97T>G , LRG_567t1:c.97T>G	NP_002464.1:p.Trp33Gly
ENST00000216181.9:c.97T>G	ENSP00000216181.5:p.Trp33Gly
ENST00000401701.1:c.97T>G	ENSP00000384631.1:p.Trp33Gly
ENST00000456729.1:c.97T>G	ENSP00000414852.1:p.Trp33Gly
ENST00000685187.1:n.311T>G
ENST00000685191.1:n.320T>G
ENST00000685801.1:c.97T>G	ENSP00000510688.1:p.Trp33Gly
ENST00000688137.1:c.97T>G	ENSP00000510189.1:p.Trp33Gly
ENST00000691296.1:c.97T>G	ENSP00000509816.1:p.Trp33Gly
ENST00000691687.1:n.311T>G
ENST00000692930.1:n.311T>G
XM_011530197.1:c.97T>G	XP_011528499.1:p.Trp33Gly
XM_011530197.2:c.97T>G	XP_011528499.1:p.Trp33Gly
XM_017028803.1:c.97T>G	XP_016884292.1:p.Trp33Gly
XM_017028804.1:c.97T>G	XP_016884293.1:p.Trp33Gly
XM_017028805.1:c.97T>G	XP_016884294.1:p.Trp33Gly
XM_017028806.1:c.97T>G	XP_016884295.1:p.Trp33Gly