Canonical Allele Identifier: CA2977871911

Gene: NTM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.131562960_131562961insAGG , CM000673.2:g.131562960_131562961insAGG	GRCh38
NC_000011.9:g.131432854_131432855insAGG , CM000673.1:g.131432854_131432855insAGG	GRCh37
NC_000011.8:g.130938064_130938065insAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001352005.2:c.82+192072_82+192073insAGG MANE Select	NP_001338934.1:n.82+192072_82+192073insAGG
ENST00000683400.1:c.82+192072_82+192073insAGG MANE Select	ENSP00000507313.1:n.82+192072_82+192073insAGG
NM_001048209.1:c.82+192072_82+192073insAGG	NP_001041674.1:n.82+192072_82+192073insAGG
NM_001048209.2:c.82+192072_82+192073insAGG	NP_001041674.1:n.82+192072_82+192073insAGG
NM_001352001.1:c.82+192072_82+192073insAGG	NP_001338930.1:n.82+192072_82+192073insAGG
NM_001352001.2:c.82+192072_82+192073insAGG	NP_001338930.1:n.82+192072_82+192073insAGG
NM_001352003.1:c.82+192072_82+192073insAGG	NP_001338932.1:n.82+192072_82+192073insAGG
NM_001352003.2:c.82+192072_82+192073insAGG	NP_001338932.1:n.82+192072_82+192073insAGG
NM_001352005.1:c.82+192072_82+192073insAGG	NP_001338934.1:n.82+192072_82+192073insAGG
NM_001352006.1:c.-65-97969_-65-97968insAGG	NP_001338935.1:n.-65-97969_-65-97968insAGG
NM_001352006.2:c.-65-97969_-65-97968insAGG	NP_001338935.1:n.-65-97969_-65-97968insAGG
NM_001352007.1:c.-65-97969_-65-97968insAGG	NP_001338936.1:n.-65-97969_-65-97968insAGG
NM_001352007.2:c.-65-97969_-65-97968insAGG	NP_001338936.1:n.-65-97969_-65-97968insAGG
NM_001386967.1:c.-42+192072_-42+192073insAGG	NP_001373896.1:n.-42+192072_-42+192073insAGG
NM_001386968.1:c.-42+192072_-42+192073insAGG	NP_001373897.1:n.-42+192072_-42+192073insAGG
NM_001386969.1:c.-42+192072_-42+192073insAGG	NP_001373898.1:n.-42+192072_-42+192073insAGG
NR_147848.1:n.413+192072_413+192073insAGG
NR_147848.2:n.274+192072_274+192073insAGG
NR_170346.1:n.275-102150_275-102149insAGG
NR_170347.1:n.274+192072_274+192073insAGG
NR_170348.1:n.274+192072_274+192073insAGG
NR_170349.1:n.274+192072_274+192073insAGG
NR_170350.1:n.274+192072_274+192073insAGG
NR_170351.1:n.275-97969_275-97968insAGG
NR_170352.1:n.275-97969_275-97968insAGG
NR_170354.1:n.274+192072_274+192073insAGG
NR_170355.1:n.274+192072_274+192073insAGG
NR_170357.1:n.274+192072_274+192073insAGG
NR_170366.1:n.274+192072_274+192073insAGG
ENST00000374791.7:c.82+192072_82+192073insAGG	ENSP00000363923.3:n.82+192072_82+192073insAGG
ENST00000436745.5:c.-65-97969_-65-97968insAGG	ENSP00000409221.1:n.-65-97969_-65-97968insAGG
ENST00000477098.1:n.261-97969_261-97968insAGG
ENST00000550167.5:c.-65-97969_-65-97968insAGG	ENSP00000448104.1:n.-65-97969_-65-97968insAGG
XM_005271580.2:c.82+192072_82+192073insAGG	XP_005271637.1:n.82+192072_82+192073insAGG
XM_005271582.2:c.82+192072_82+192073insAGG	XP_005271639.1:n.82+192072_82+192073insAGG
XM_006718854.2:c.-65-97969_-65-97968insAGG	XP_006718917.1:n.-65-97969_-65-97968insAGG
XM_006718855.2:c.-65-97969_-65-97968insAGG	XP_006718918.1:n.-65-97969_-65-97968insAGG
XM_017017852.2:c.82+192072_82+192073insAGG	XP_016873341.1:n.82+192072_82+192073insAGG
XM_017017855.2:c.82+192072_82+192073insAGG	XP_016873344.1:n.82+192072_82+192073insAGG
XM_017017865.2:c.82+192072_82+192073insAGG	XP_016873354.1:n.82+192072_82+192073insAGG
XR_001747894.2:n.581+192072_581+192073insAGG