Canonical Allele Identifier: CA915951363

Gene: MYH9

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282788_36282799dup , CM000684.2:g.36282788_36282799dup	GRCh38
NC_000022.10:g.36678834_36678845dup , CM000684.1:g.36678834_36678845dup	GRCh37
NC_000022.9:g.35008780_35008791dup	NCBI36
NG_011884.2:g.110221_110232dup , LRG_567:g.110221_110232dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2199-13_2199-2dup
ENST00000685801.1:c.5829-13_5829-2dup	ENSP00000510688.1:n.5829-13_5829-2dup
ENST00000690244.1:n.1102-13_1102-2dup
ENST00000691109.1:n.6061-13_6061-2dup
ENST00000216181.11:c.5766-13_5766-2dup MANE Select	ENSP00000216181.6:n.5766-13_5766-2dup
ENST00000216181.9:c.5766-13_5766-2dup	ENSP00000216181.5:n.5766-13_5766-2dup
NM_002473.5:c.5766-13_5766-2dup , LRG_567t1:c.5766-13_5766-2dup	NP_002464.1:n.5766-13_5766-2dup
XM_011530197.1:c.5766-13_5766-2dup	XP_011528499.1:n.5766-13_5766-2dup
XM_011530197.2:c.5766-13_5766-2dup	XP_011528499.1:n.5766-13_5766-2dup
XM_017028803.1:c.5766-13_5766-2dup	XP_016884292.1:n.5766-13_5766-2dup
XM_017028804.1:c.5766-13_5766-2dup	XP_016884293.1:n.5766-13_5766-2dup
XM_017028805.1:c.5766-13_5766-2dup	XP_016884294.1:n.5766-13_5766-2dup
XM_017028806.1:c.5766-13_5766-2dup	XP_016884295.1:n.5766-13_5766-2dup
NM_002473.6:c.5766-13_5766-2dup MANE Select	NP_002464.1:n.5766-13_5766-2dup