Canonical Allele Identifier: CA2656426645

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282178-T-TAGAAGCAGAGGGTCAGCGGGCCCGGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282178_36282179insAGAAGCAGAGGGTCAGCGGGCCCGGCCA , CM000684.2:g.36282178_36282179insAGAAGCAGAGGGTCAGCGGGCCCGGCCA	GRCh38
NC_000022.10:g.36678224_36678225insAGAAGCAGAGGGTCAGCGGGCCCGGCCA , CM000684.1:g.36678224_36678225insAGAAGCAGAGGGTCAGCGGGCCCGGCCA	GRCh37
NC_000022.9:g.35008170_35008171insAGAAGCAGAGGGTCAGCGGGCCCGGCCA	NCBI36
NG_011884.2:g.110840_110841insTGGCCGGGCCCGCTGACCCTCTGCTTCT , LRG_567:g.110840_110841insTGGCCGGGCCCGCTGACCCTCTGCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2805_2806insTGGCCGGGCCCGCTGACCCTCTGCTTCT
ENST00000685801.1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	ENSP00000510688.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
ENST00000690244.1:n.1708_1709insTGGCCGGGCCCGCTGACCCTCTGCTTCT
ENST00000691109.1:n.6667_6668insTGGCCGGGCCCGCTGACCCTCTGCTTCT
ENST00000216181.11:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT MANE Select	ENSP00000216181.6:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
ENST00000216181.9:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	ENSP00000216181.5:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
NM_002473.5:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT , LRG_567t1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	NP_002464.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
XM_011530197.1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	XP_011528499.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
XM_011530197.2:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	XP_011528499.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
XM_017028803.1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	XP_016884292.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
XM_017028804.1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	XP_016884293.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
XM_017028805.1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	XP_016884294.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
XM_017028806.1:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT	XP_016884295.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT
NM_002473.6:c.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT MANE Select	NP_002464.1:n.*489_*490insTGGCCGGGCCCGCTGACCCTCTGCTTCT