Canonical Allele Identifier: CA2186535859

Gene: MYO9A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71877129_71877133delinsCTAAT , CM000677.2:g.71877129_71877133delinsCTAAT	GRCh38
NC_000015.9:g.72169470_72169474delinsCTAAT , CM000677.1:g.72169470_72169474delinsCTAAT	GRCh37
NC_000015.8:g.69956524_69956528delinsCTAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356056.10:c.5931+907_5931+911delinsATTAG MANE Select	ENSP00000348349.5:n.5931+907_5931+911delinsATTAG
ENST00000356056.9:c.5931+907_5931+911delinsATTAG	ENSP00000348349.5:n.5931+907_5931+911delinsATTAG
ENST00000444904.5:c.5931+907_5931+911delinsATTAG	ENSP00000398250.2:n.5931+907_5931+911delinsATTAG
ENST00000561618.5:c.2480+907_2480+911delinsATTAG
ENST00000564571.5:c.5931+907_5931+911delinsATTAG	ENSP00000456192.1:n.5931+907_5931+911delinsATTAG
NM_006901.3:c.5931+907_5931+911delinsATTAG	NP_008832.2:n.5931+907_5931+911delinsATTAG
XM_006720539.1:c.6144+907_6144+911delinsATTAG	XP_006720602.1:n.6144+907_6144+911delinsATTAG
XM_011521613.1:c.6147+907_6147+911delinsATTAG	XP_011519915.1:n.6147+907_6147+911delinsATTAG
XM_011521614.1:c.6147+907_6147+911delinsATTAG	XP_011519916.1:n.6147+907_6147+911delinsATTAG
XM_011521615.1:c.6147+907_6147+911delinsATTAG	XP_011519917.1:n.6147+907_6147+911delinsATTAG
XM_011521616.1:c.6147+907_6147+911delinsATTAG	XP_011519918.1:n.6147+907_6147+911delinsATTAG
XM_011521617.1:c.6144+907_6144+911delinsATTAG	XP_011519919.1:n.6144+907_6144+911delinsATTAG
XM_011521618.1:c.6147+907_6147+911delinsATTAG	XP_011519920.1:n.6147+907_6147+911delinsATTAG
XM_011521619.1:c.6090+907_6090+911delinsATTAG	XP_011519921.1:n.6090+907_6090+911delinsATTAG
XM_011521620.1:c.6087+907_6087+911delinsATTAG	XP_011519922.1:n.6087+907_6087+911delinsATTAG
XM_011521621.1:c.6027+907_6027+911delinsATTAG	XP_011519923.1:n.6027+907_6027+911delinsATTAG
XM_011521622.1:c.5931+907_5931+911delinsATTAG	XP_011519924.1:n.5931+907_5931+911delinsATTAG
XM_011521623.1:c.3444+907_3444+911delinsATTAG	XP_011519925.1:n.3444+907_3444+911delinsATTAG
XM_006720539.3:c.6144+907_6144+911delinsATTAG	XP_006720602.1:n.6144+907_6144+911delinsATTAG
XM_011521613.3:c.6147+907_6147+911delinsATTAG	XP_011519915.1:n.6147+907_6147+911delinsATTAG
XM_011521614.3:c.6147+907_6147+911delinsATTAG	XP_011519916.1:n.6147+907_6147+911delinsATTAG
XM_011521615.3:c.6147+907_6147+911delinsATTAG	XP_011519917.1:n.6147+907_6147+911delinsATTAG
XM_011521616.3:c.6147+907_6147+911delinsATTAG	XP_011519918.1:n.6147+907_6147+911delinsATTAG
XM_011521617.3:c.6144+907_6144+911delinsATTAG	XP_011519919.1:n.6144+907_6144+911delinsATTAG
XM_011521618.3:c.6147+907_6147+911delinsATTAG	XP_011519920.1:n.6147+907_6147+911delinsATTAG
XM_011521619.3:c.6090+907_6090+911delinsATTAG	XP_011519921.1:n.6090+907_6090+911delinsATTAG
XM_011521620.3:c.6087+907_6087+911delinsATTAG	XP_011519922.1:n.6087+907_6087+911delinsATTAG
XM_011521621.3:c.6027+907_6027+911delinsATTAG	XP_011519923.1:n.6027+907_6027+911delinsATTAG
XM_011521622.3:c.5931+907_5931+911delinsATTAG	XP_011519924.1:n.5931+907_5931+911delinsATTAG
XM_011521623.3:c.3444+907_3444+911delinsATTAG	XP_011519925.1:n.3444+907_3444+911delinsATTAG
XM_017022229.1:c.5931+907_5931+911delinsATTAG	XP_016877718.1:n.5931+907_5931+911delinsATTAG
XM_017022230.2:c.5874+907_5874+911delinsATTAG	XP_016877719.1:n.5874+907_5874+911delinsATTAG
NM_006901.4:c.5931+907_5931+911delinsATTAG MANE Select	NP_008832.2:n.5931+907_5931+911delinsATTAG