Canonical Allele Identifier: CA2656426650

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282178-T-TAGAAGCAGAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282178_36282179insAGAAGCAGAGG , CM000684.2:g.36282178_36282179insAGAAGCAGAGG	GRCh38
NC_000022.10:g.36678224_36678225insAGAAGCAGAGG , CM000684.1:g.36678224_36678225insAGAAGCAGAGG	GRCh37
NC_000022.9:g.35008170_35008171insAGAAGCAGAGG	NCBI36
NG_011884.2:g.110840_110841insCCTCTGCTTCT , LRG_567:g.110840_110841insCCTCTGCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2805_2806insCCTCTGCTTCT
ENST00000685801.1:c.*489_*490insCCTCTGCTTCT	ENSP00000510688.1:n.*489_*490insCCTCTGCTTCT
ENST00000690244.1:n.1708_1709insCCTCTGCTTCT
ENST00000691109.1:n.6667_6668insCCTCTGCTTCT
ENST00000216181.11:c.*489_*490insCCTCTGCTTCT MANE Select	ENSP00000216181.6:n.*489_*490insCCTCTGCTTCT
ENST00000216181.9:c.*489_*490insCCTCTGCTTCT	ENSP00000216181.5:n.*489_*490insCCTCTGCTTCT
NM_002473.5:c.*489_*490insCCTCTGCTTCT , LRG_567t1:c.*489_*490insCCTCTGCTTCT	NP_002464.1:n.*489_*490insCCTCTGCTTCT
XM_011530197.1:c.*489_*490insCCTCTGCTTCT	XP_011528499.1:n.*489_*490insCCTCTGCTTCT
XM_011530197.2:c.*489_*490insCCTCTGCTTCT	XP_011528499.1:n.*489_*490insCCTCTGCTTCT
XM_017028803.1:c.*489_*490insCCTCTGCTTCT	XP_016884292.1:n.*489_*490insCCTCTGCTTCT
XM_017028804.1:c.*489_*490insCCTCTGCTTCT	XP_016884293.1:n.*489_*490insCCTCTGCTTCT
XM_017028805.1:c.*489_*490insCCTCTGCTTCT	XP_016884294.1:n.*489_*490insCCTCTGCTTCT
XM_017028806.1:c.*489_*490insCCTCTGCTTCT	XP_016884295.1:n.*489_*490insCCTCTGCTTCT
NM_002473.6:c.*489_*490insCCTCTGCTTCT MANE Select	NP_002464.1:n.*489_*490insCCTCTGCTTCT