Canonical Allele Identifier: CA1764810615

Gene: TRMT9B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.12953715_12953718delinsACTG , CM000670.2:g.12953715_12953718delinsACTG	GRCh38
NC_000008.10:g.12811224_12811227delinsACTG , CM000670.1:g.12811224_12811227delinsACTG	GRCh37
NC_000008.9:g.12855595_12855598delinsACTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528335.6:c.-200+1357_-200+1360delinsACTG	ENSP00000518785.1:n.-200+1357_-200+1360delinsACTG
ENST00000524591.7:c.-200+7749_-200+7752delinsACTG MANE Select	ENSP00000432695.1:n.-200+7749_-200+7752delinsACTG
ENST00000400069.7:c.-169+1357_-169+1360delinsACTG	ENSP00000468715.1:n.-169+1357_-169+1360delinsACTG
ENST00000447063.6:c.-200+7749_-200+7752delinsACTG	ENSP00000443288.1:n.-200+7749_-200+7752delinsACTG
ENST00000524591.6:c.-200+7749_-200+7752delinsACTG	ENSP00000432695.1:n.-200+7749_-200+7752delinsACTG
ENST00000525249.1:n.293+7749_293+7752delinsACTG
ENST00000528335.5:n.349+1357_349+1360delinsACTG
ENST00000528753.2:c.-200+1357_-200+1360delinsACTG	ENSP00000466330.1:n.-200+1357_-200+1360delinsACTG
ENST00000532376.2:c.-169+1357_-169+1360delinsACTG	ENSP00000431717.2:n.-169+1357_-169+1360delinsACTG
NM_020844.2:c.-200+7749_-200+7752delinsACTG	NP_065895.2:n.-200+7749_-200+7752delinsACTG
XM_005273584.3:c.39+1011_39+1014delinsACTG	XP_005273641.1:n.39+1011_39+1014delinsACTG
XM_005273585.3:c.-109+1357_-109+1360delinsACTG	XP_005273642.1:n.-109+1357_-109+1360delinsACTG
XM_005273586.3:c.-200+1357_-200+1360delinsACTG	XP_005273643.1:n.-200+1357_-200+1360delinsACTG
XM_011544596.1:c.254+1357_254+1360delinsACTG	XP_011542898.1:n.254+1357_254+1360delinsACTG
XM_011544597.1:c.254+1357_254+1360delinsACTG	XP_011542899.1:n.254+1357_254+1360delinsACTG
XM_011544598.1:c.-109+1357_-109+1360delinsACTG	XP_011542900.1:n.-109+1357_-109+1360delinsACTG
XM_011544599.1:c.-1984-886_-1984-883delinsACTG	XP_011542901.1:n.-1984-886_-1984-883delinsACTG
XM_011544601.1:c.-109+7749_-109+7752delinsACTG	XP_011542903.1:n.-109+7749_-109+7752delinsACTG
XM_005273584.5:c.39+1011_39+1014delinsACTG	XP_005273641.1:n.39+1011_39+1014delinsACTG
XM_005273585.4:c.-109+1357_-109+1360delinsACTG	XP_005273642.1:n.-109+1357_-109+1360delinsACTG
XM_005273586.4:c.-200+1357_-200+1360delinsACTG	XP_005273643.1:n.-200+1357_-200+1360delinsACTG
XM_005273588.5:c.-378+1357_-378+1360delinsACTG	XP_005273645.1:n.-378+1357_-378+1360delinsACTG
XM_005273591.5:c.-409+1357_-409+1360delinsACTG	XP_005273648.1:n.-409+1357_-409+1360delinsACTG
XM_011544596.3:c.254+1357_254+1360delinsACTG	XP_011542898.1:n.254+1357_254+1360delinsACTG
XM_011544597.3:c.254+1357_254+1360delinsACTG	XP_011542899.1:n.254+1357_254+1360delinsACTG
XM_011544598.2:c.-109+1357_-109+1360delinsACTG	XP_011542900.1:n.-109+1357_-109+1360delinsACTG
XM_011544601.3:c.-109+7749_-109+7752delinsACTG	XP_011542903.1:n.-109+7749_-109+7752delinsACTG
XM_017013706.2:c.-200+1011_-200+1014delinsACTG	XP_016869195.1:n.-200+1011_-200+1014delinsACTG
XM_017013710.1:c.-434+1357_-434+1360delinsACTG	XP_016869199.1:n.-434+1357_-434+1360delinsACTG
XM_017013714.2:c.-306+1357_-306+1360delinsACTG	XP_016869203.1:n.-306+1357_-306+1360delinsACTG
XM_024447214.1:c.-263+1357_-263+1360delinsACTG	XP_024302982.1:n.-263+1357_-263+1360delinsACTG
XM_024447215.1:c.-354+1357_-354+1360delinsACTG	XP_024302983.1:n.-354+1357_-354+1360delinsACTG
XM_024447216.1:c.-378+1357_-378+1360delinsACTG	XP_024302984.1:n.-378+1357_-378+1360delinsACTG
XM_024447219.1:c.-1098+1357_-1098+1360delinsACTG	XP_024302987.1:n.-1098+1357_-1098+1360delinsACTG
NM_020844.3:c.-200+7749_-200+7752delinsACTG MANE Select	NP_065895.2:n.-200+7749_-200+7752delinsACTG