Canonical Allele Identifier: CA2656426627

Gene: MYH9

Linked Data

• gnomAD v4: 22-36282167-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282167_36282168insT , CM000684.2:g.36282167_36282168insT	GRCh38
NC_000022.10:g.36678213_36678214insT , CM000684.1:g.36678213_36678214insT	GRCh37
NC_000022.9:g.35008159_35008160insT	NCBI36
NG_011884.2:g.110851_110852insA , LRG_567:g.110851_110852insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2816_2817insA
ENST00000685801.1:c.*500_*501insA	ENSP00000510688.1:n.*500_*501insA
ENST00000690244.1:n.1719_1720insA
ENST00000691109.1:n.6678_6679insA
ENST00000216181.11:c.*500_*501insA MANE Select	ENSP00000216181.6:n.*500_*501insA
ENST00000216181.9:c.*500_*501insA	ENSP00000216181.5:n.*500_*501insA
NM_002473.5:c.*500_*501insA , LRG_567t1:c.*500_*501insA	NP_002464.1:n.*500_*501insA
XM_011530197.1:c.*500_*501insA	XP_011528499.1:n.*500_*501insA
XM_011530197.2:c.*500_*501insA	XP_011528499.1:n.*500_*501insA
XM_017028803.1:c.*500_*501insA	XP_016884292.1:n.*500_*501insA
XM_017028804.1:c.*500_*501insA	XP_016884293.1:n.*500_*501insA
XM_017028805.1:c.*500_*501insA	XP_016884294.1:n.*500_*501insA
XM_017028806.1:c.*500_*501insA	XP_016884295.1:n.*500_*501insA
NM_002473.6:c.*500_*501insA MANE Select	NP_002464.1:n.*500_*501insA