Canonical Allele Identifier: CA2656426649

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282178-T-TAGAAGCAGAGGGTCAGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282178_36282179insAGAAGCAGAGGGTCAGCG , CM000684.2:g.36282178_36282179insAGAAGCAGAGGGTCAGCG	GRCh38
NC_000022.10:g.36678224_36678225insAGAAGCAGAGGGTCAGCG , CM000684.1:g.36678224_36678225insAGAAGCAGAGGGTCAGCG	GRCh37
NC_000022.9:g.35008170_35008171insAGAAGCAGAGGGTCAGCG	NCBI36
NG_011884.2:g.110840_110841insCGCTGACCCTCTGCTTCT , LRG_567:g.110840_110841insCGCTGACCCTCTGCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2805_2806insCGCTGACCCTCTGCTTCT
ENST00000685801.1:c.*489_*490insCGCTGACCCTCTGCTTCT	ENSP00000510688.1:n.*489_*490insCGCTGACCCTCTGCTTCT
ENST00000690244.1:n.1708_1709insCGCTGACCCTCTGCTTCT
ENST00000691109.1:n.6667_6668insCGCTGACCCTCTGCTTCT
ENST00000216181.11:c.*489_*490insCGCTGACCCTCTGCTTCT MANE Select	ENSP00000216181.6:n.*489_*490insCGCTGACCCTCTGCTTCT
ENST00000216181.9:c.*489_*490insCGCTGACCCTCTGCTTCT	ENSP00000216181.5:n.*489_*490insCGCTGACCCTCTGCTTCT
NM_002473.5:c.*489_*490insCGCTGACCCTCTGCTTCT , LRG_567t1:c.*489_*490insCGCTGACCCTCTGCTTCT	NP_002464.1:n.*489_*490insCGCTGACCCTCTGCTTCT
XM_011530197.1:c.*489_*490insCGCTGACCCTCTGCTTCT	XP_011528499.1:n.*489_*490insCGCTGACCCTCTGCTTCT
XM_011530197.2:c.*489_*490insCGCTGACCCTCTGCTTCT	XP_011528499.1:n.*489_*490insCGCTGACCCTCTGCTTCT
XM_017028803.1:c.*489_*490insCGCTGACCCTCTGCTTCT	XP_016884292.1:n.*489_*490insCGCTGACCCTCTGCTTCT
XM_017028804.1:c.*489_*490insCGCTGACCCTCTGCTTCT	XP_016884293.1:n.*489_*490insCGCTGACCCTCTGCTTCT
XM_017028805.1:c.*489_*490insCGCTGACCCTCTGCTTCT	XP_016884294.1:n.*489_*490insCGCTGACCCTCTGCTTCT
XM_017028806.1:c.*489_*490insCGCTGACCCTCTGCTTCT	XP_016884295.1:n.*489_*490insCGCTGACCCTCTGCTTCT
NM_002473.6:c.*489_*490insCGCTGACCCTCTGCTTCT MANE Select	NP_002464.1:n.*489_*490insCGCTGACCCTCTGCTTCT