Canonical Allele Identifier: CA2009506913

Gene: NTM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.131480993_131481001delinsGGGGTAGAA , CM000673.2:g.131480993_131481001delinsGGGGTAGAA	GRCh38
NC_000011.9:g.131350887_131350895delinsGGGGTAGAA , CM000673.1:g.131350887_131350895delinsGGGGTAGAA	GRCh37
NC_000011.8:g.130856097_130856105delinsGGGGTAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000683400.1:c.82+110105_82+110113delinsGGGGTAGAA MANE Select	ENSP00000507313.1:n.82+110105_82+110113delinsGGGGTAGAA
ENST00000374791.7:c.82+110105_82+110113delinsGGGGTAGAA	ENSP00000363923.3:n.82+110105_82+110113delinsGGGGTAGAA
ENST00000436745.5:c.-66+110105_-66+110113delinsGGGGTAGAA	ENSP00000409221.1:n.-66+110105_-66+110113delinsGGGGTAGAA
ENST00000477098.1:n.260+110105_260+110113delinsGGGGTAGAA
ENST00000550167.5:c.-66+25526_-66+25534delinsGGGGTAGAA	ENSP00000448104.1:n.-66+25526_-66+25534delinsGGGGTAGAA
NM_001048209.1:c.82+110105_82+110113delinsGGGGTAGAA	NP_001041674.1:n.82+110105_82+110113delinsGGGGTAGAA
XM_005271580.2:c.82+110105_82+110113delinsGGGGTAGAA	XP_005271637.1:n.82+110105_82+110113delinsGGGGTAGAA
XM_005271582.2:c.82+110105_82+110113delinsGGGGTAGAA	XP_005271639.1:n.82+110105_82+110113delinsGGGGTAGAA
XM_006718854.2:c.-66+110105_-66+110113delinsGGGGTAGAA	XP_006718917.1:n.-66+110105_-66+110113delinsGGGGTAGAA
XM_006718855.2:c.-66+110105_-66+110113delinsGGGGTAGAA	XP_006718918.1:n.-66+110105_-66+110113delinsGGGGTAGAA
NM_001352001.1:c.82+110105_82+110113delinsGGGGTAGAA	NP_001338930.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352003.1:c.82+110105_82+110113delinsGGGGTAGAA	NP_001338932.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352005.1:c.82+110105_82+110113delinsGGGGTAGAA	NP_001338934.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352006.1:c.-66+110105_-66+110113delinsGGGGTAGAA	NP_001338935.1:n.-66+110105_-66+110113delinsGGGGTAGAA
NM_001352007.1:c.-66+110105_-66+110113delinsGGGGTAGAA	NP_001338936.1:n.-66+110105_-66+110113delinsGGGGTAGAA
NR_147848.1:n.413+110105_413+110113delinsGGGGTAGAA
XM_017017852.2:c.82+110105_82+110113delinsGGGGTAGAA	XP_016873341.1:n.82+110105_82+110113delinsGGGGTAGAA
XM_017017855.2:c.82+110105_82+110113delinsGGGGTAGAA	XP_016873344.1:n.82+110105_82+110113delinsGGGGTAGAA
XM_017017865.2:c.82+110105_82+110113delinsGGGGTAGAA	XP_016873354.1:n.82+110105_82+110113delinsGGGGTAGAA
XR_001747894.2:n.581+110105_581+110113delinsGGGGTAGAA
NM_001048209.2:c.82+110105_82+110113delinsGGGGTAGAA	NP_001041674.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352001.2:c.82+110105_82+110113delinsGGGGTAGAA	NP_001338930.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352003.2:c.82+110105_82+110113delinsGGGGTAGAA	NP_001338932.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352005.2:c.82+110105_82+110113delinsGGGGTAGAA MANE Select	NP_001338934.1:n.82+110105_82+110113delinsGGGGTAGAA
NM_001352006.2:c.-66+110105_-66+110113delinsGGGGTAGAA	NP_001338935.1:n.-66+110105_-66+110113delinsGGGGTAGAA
NM_001352007.2:c.-66+110105_-66+110113delinsGGGGTAGAA	NP_001338936.1:n.-66+110105_-66+110113delinsGGGGTAGAA
NR_147848.2:n.274+110105_274+110113delinsGGGGTAGAA
NM_001386967.1:c.-42+110105_-42+110113delinsGGGGTAGAA	NP_001373896.1:n.-42+110105_-42+110113delinsGGGGTAGAA
NM_001386968.1:c.-42+110105_-42+110113delinsGGGGTAGAA	NP_001373897.1:n.-42+110105_-42+110113delinsGGGGTAGAA
NM_001386969.1:c.-42+110105_-42+110113delinsGGGGTAGAA	NP_001373898.1:n.-42+110105_-42+110113delinsGGGGTAGAA
NR_170346.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170347.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170348.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170349.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170350.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170351.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170352.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170354.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170355.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170357.1:n.274+110105_274+110113delinsGGGGTAGAA
NR_170366.1:n.274+110105_274+110113delinsGGGGTAGAA