Canonical Allele Identifier: CA2656426671

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282193-CGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282197_36282198del , CM000684.2:g.36282197_36282198del	GRCh38
NC_000022.10:g.36678243_36678244del , CM000684.1:g.36678243_36678244del	GRCh37
NC_000022.9:g.35008189_35008190del	NCBI36
NG_011884.2:g.110824_110825del , LRG_567:g.110824_110825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2789_2790del
ENST00000685801.1:c.*473_*474del	ENSP00000510688.1:n.*473_*474del
ENST00000690244.1:n.1692_1693del
ENST00000691109.1:n.6651_6652del
ENST00000216181.11:c.*473_*474del MANE Select	ENSP00000216181.6:n.*473_*474del
ENST00000216181.9:c.*473_*474del	ENSP00000216181.5:n.*473_*474del
NM_002473.5:c.*473_*474del , LRG_567t1:c.*473_*474del	NP_002464.1:n.*473_*474del
XM_011530197.1:c.*473_*474del	XP_011528499.1:n.*473_*474del
XM_011530197.2:c.*473_*474del	XP_011528499.1:n.*473_*474del
XM_017028803.1:c.*473_*474del	XP_016884292.1:n.*473_*474del
XM_017028804.1:c.*473_*474del	XP_016884293.1:n.*473_*474del
XM_017028805.1:c.*473_*474del	XP_016884294.1:n.*473_*474del
XM_017028806.1:c.*473_*474del	XP_016884295.1:n.*473_*474del
NM_002473.6:c.*473_*474del MANE Select	NP_002464.1:n.*473_*474del