Canonical Allele Identifier: CA639373627

Gene: MYH9

Linked Data

• gnomAD v2: 22-36751045-CAG-C
• gnomAD v3: 22-36355000-CAG-C
• gnomAD v4: 22-36355000-CAG-C
• MyVariant Identifiers: chr22:g.36751046_36751047del (hg19) ; chr22:g.36355001_36355002del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36355003_36355004del , CM000684.2:g.36355003_36355004del	GRCh38
NC_000022.10:g.36751048_36751049del , CM000684.1:g.36751048_36751049del	GRCh37
NC_000022.9:g.35080994_35080995del	NCBI36
NG_011884.2:g.38017_38018del , LRG_567:g.38017_38018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685187.1:n.196-5747_196-5746del
ENST00000685191.1:n.205-5747_205-5746del
ENST00000685801.1:c.-19-5747_-19-5746del	ENSP00000510688.1:n.-19-5747_-19-5746del
ENST00000688137.1:c.-19-5747_-19-5746del	ENSP00000510189.1:n.-19-5747_-19-5746del
ENST00000691296.1:c.-19-5747_-19-5746del	ENSP00000509816.1:n.-19-5747_-19-5746del
ENST00000691687.1:n.196-5747_196-5746del
ENST00000692930.1:n.196-5747_196-5746del
ENST00000216181.11:c.-19-5747_-19-5746del MANE Select	ENSP00000216181.6:n.-19-5747_-19-5746del
ENST00000216181.9:c.-19-5747_-19-5746del	ENSP00000216181.5:n.-19-5747_-19-5746del
ENST00000401701.1:c.-19-5747_-19-5746del	ENSP00000384631.1:n.-19-5747_-19-5746del
ENST00000456729.1:c.-19-5747_-19-5746del	ENSP00000414852.1:n.-19-5747_-19-5746del
NM_002473.5:c.-19-5747_-19-5746del , LRG_567t1:c.-19-5747_-19-5746del	NP_002464.1:n.-19-5747_-19-5746del
XM_011530197.1:c.-19-5747_-19-5746del	XP_011528499.1:n.-19-5747_-19-5746del
XM_011530197.2:c.-19-5747_-19-5746del	XP_011528499.1:n.-19-5747_-19-5746del
XM_017028803.1:c.-19-5747_-19-5746del	XP_016884292.1:n.-19-5747_-19-5746del
XM_017028804.1:c.-19-5747_-19-5746del	XP_016884293.1:n.-19-5747_-19-5746del
XM_017028806.1:c.-19-5747_-19-5746del	XP_016884295.1:n.-19-5747_-19-5746del
NM_002473.6:c.-19-5747_-19-5746del MANE Select	NP_002464.1:n.-19-5747_-19-5746del