Canonical Allele Identifier: CA2403794994

Gene: MYH9

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36282080_36282081delinsAC , CM000684.2:g.36282080_36282081delinsAC	GRCh38
NC_000022.10:g.36678126_36678127delinsAC , CM000684.1:g.36678126_36678127delinsAC	GRCh37
NC_000022.9:g.35008072_35008073delinsAC	NCBI36
NG_011884.2:g.110938_110939delinsGT , LRG_567:g.110938_110939delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685708.1:n.2903_2904delinsGT
ENST00000685801.1:c.*587_*588delinsGT	ENSP00000510688.1:n.*587_*588delinsGT
ENST00000690244.1:n.1806_1807delinsGT
ENST00000691109.1:n.6765_6766delinsGT
ENST00000216181.11:c.*587_*588delinsGT MANE Select	ENSP00000216181.6:n.*587_*588delinsGT
ENST00000216181.9:c.*587_*588delinsGT	ENSP00000216181.5:n.*587_*588delinsGT
NM_002473.5:c.*587_*588delinsGT , LRG_567t1:c.*587_*588delinsGT	NP_002464.1:n.*587_*588delinsGT
XM_011530197.1:c.*587_*588delinsGT	XP_011528499.1:n.*587_*588delinsGT
XM_011530197.2:c.*587_*588delinsGT	XP_011528499.1:n.*587_*588delinsGT
XM_017028803.1:c.*587_*588delinsGT	XP_016884292.1:n.*587_*588delinsGT
XM_017028804.1:c.*587_*588delinsGT	XP_016884293.1:n.*587_*588delinsGT
XM_017028805.1:c.*587_*588delinsGT	XP_016884294.1:n.*587_*588delinsGT
XM_017028806.1:c.*587_*588delinsGT	XP_016884295.1:n.*587_*588delinsGT
NM_002473.6:c.*587_*588delinsGT MANE Select	NP_002464.1:n.*587_*588delinsGT