Canonical Allele Identifier: CA2403814413

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36322407G= , CM000684.2:g.36322407G=	GRCh38
NC_000022.10:g.36718452G= , CM000684.1:g.36718452G=	GRCh37
NC_000022.9:g.35048398G=	NCBI36
NG_011884.2:g.70612C= , LRG_567:g.70612C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000685187.1:n.919+22C=
ENST00000685191.1:n.928+22C=
ENST00000685801.1:c.705+22C=	ENSP00000510688.1:n.705+22C=
ENST00000691109.1:n.566+22C=
ENST00000691687.1:n.919+22C=
ENST00000692930.1:n.919+22C=
ENST00000216181.11:c.705+22C= MANE Select	ENSP00000216181.6:n.705+22C=
ENST00000216181.9:c.705+22C=	ENSP00000216181.5:n.705+22C=
ENST00000463027.1:n.309+22C=
NM_002473.5:c.705+22C= , LRG_567t1:c.705+22C=	NP_002464.1:n.705+22C=
XM_011530197.1:c.705+22C=	XP_011528499.1:n.705+22C=
XM_011530197.2:c.705+22C=	XP_011528499.1:n.705+22C=
XM_017028803.1:c.705+22C=	XP_016884292.1:n.705+22C=
XM_017028804.1:c.705+22C=	XP_016884293.1:n.705+22C=
XM_017028805.1:c.705+22C=	XP_016884294.1:n.705+22C=
XM_017028806.1:c.705+22C=	XP_016884295.1:n.705+22C=
NM_002473.6:c.705+22C= MANE Select	NP_002464.1:n.705+22C=