Canonical Allele Identifier: CA10208889

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282700C>T , CM000684.2:g.36282700C>T	GRCh38
NC_000022.10:g.36678746C>T , CM000684.1:g.36678746C>T	GRCh37
NC_000022.9:g.35008692C>T	NCBI36
NG_011884.2:g.110319G>A , LRG_567:g.110319G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002473.6:c.5851G>A MANE Select	NP_002464.1:p.Ala1951Thr
ENST00000216181.11:c.5851G>A MANE Select	ENSP00000216181.6:p.Ala1951Thr
NM_002473.5:c.5851G>A , LRG_567t1:c.5851G>A	NP_002464.1:p.Ala1951Thr
ENST00000216181.9:c.5851G>A	ENSP00000216181.5:p.Ala1951Thr
ENST00000685708.1:n.2284G>A
ENST00000685801.1:c.5914G>A	ENSP00000510688.1:p.Ala1972Thr
ENST00000690244.1:n.1187G>A
ENST00000691109.1:n.6146G>A
XM_011530197.1:c.5851G>A	XP_011528499.1:p.Ala1951Thr
XM_011530197.2:c.5851G>A	XP_011528499.1:p.Ala1951Thr
XM_017028803.1:c.5851G>A	XP_016884292.1:p.Ala1951Thr
XM_017028804.1:c.5851G>A	XP_016884293.1:p.Ala1951Thr
XM_017028805.1:c.5851G>A	XP_016884294.1:p.Ala1951Thr
XM_017028806.1:c.5851G>A	XP_016884295.1:p.Ala1951Thr