Canonical Allele Identifier: CA1764810636

Gene: TRMT9B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.12953723_12953727delinsGTGTT , CM000670.2:g.12953723_12953727delinsGTGTT	GRCh38
NC_000008.10:g.12811232_12811236delinsGTGTT , CM000670.1:g.12811232_12811236delinsGTGTT	GRCh37
NC_000008.9:g.12855603_12855607delinsGTGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528335.6:c.-200+1365_-200+1369delinsGTGTT	ENSP00000518785.1:n.-200+1365_-200+1369delinsGTGTT
ENST00000524591.7:c.-200+7757_-200+7761delinsGTGTT MANE Select	ENSP00000432695.1:n.-200+7757_-200+7761delinsGTGTT
ENST00000400069.7:c.-169+1365_-169+1369delinsGTGTT	ENSP00000468715.1:n.-169+1365_-169+1369delinsGTGTT
ENST00000447063.6:c.-200+7757_-200+7761delinsGTGTT	ENSP00000443288.1:n.-200+7757_-200+7761delinsGTGTT
ENST00000524591.6:c.-200+7757_-200+7761delinsGTGTT	ENSP00000432695.1:n.-200+7757_-200+7761delinsGTGTT
ENST00000525249.1:n.293+7757_293+7761delinsGTGTT
ENST00000528335.5:n.349+1365_349+1369delinsGTGTT
ENST00000528753.2:c.-200+1365_-200+1369delinsGTGTT	ENSP00000466330.1:n.-200+1365_-200+1369delinsGTGTT
ENST00000532376.2:c.-169+1365_-169+1369delinsGTGTT	ENSP00000431717.2:n.-169+1365_-169+1369delinsGTGTT
NM_020844.2:c.-200+7757_-200+7761delinsGTGTT	NP_065895.2:n.-200+7757_-200+7761delinsGTGTT
XM_005273584.3:c.39+1019_39+1023delinsGTGTT	XP_005273641.1:n.39+1019_39+1023delinsGTGTT
XM_005273585.3:c.-109+1365_-109+1369delinsGTGTT	XP_005273642.1:n.-109+1365_-109+1369delinsGTGTT
XM_005273586.3:c.-200+1365_-200+1369delinsGTGTT	XP_005273643.1:n.-200+1365_-200+1369delinsGTGTT
XM_011544596.1:c.254+1365_254+1369delinsGTGTT	XP_011542898.1:n.254+1365_254+1369delinsGTGTT
XM_011544597.1:c.254+1365_254+1369delinsGTGTT	XP_011542899.1:n.254+1365_254+1369delinsGTGTT
XM_011544598.1:c.-109+1365_-109+1369delinsGTGTT	XP_011542900.1:n.-109+1365_-109+1369delinsGTGTT
XM_011544599.1:c.-1984-878_-1984-874delinsGTGTT	XP_011542901.1:n.-1984-878_-1984-874delinsGTGTT
XM_011544601.1:c.-109+7757_-109+7761delinsGTGTT	XP_011542903.1:n.-109+7757_-109+7761delinsGTGTT
XM_005273584.5:c.39+1019_39+1023delinsGTGTT	XP_005273641.1:n.39+1019_39+1023delinsGTGTT
XM_005273585.4:c.-109+1365_-109+1369delinsGTGTT	XP_005273642.1:n.-109+1365_-109+1369delinsGTGTT
XM_005273586.4:c.-200+1365_-200+1369delinsGTGTT	XP_005273643.1:n.-200+1365_-200+1369delinsGTGTT
XM_005273588.5:c.-378+1365_-378+1369delinsGTGTT	XP_005273645.1:n.-378+1365_-378+1369delinsGTGTT
XM_005273591.5:c.-409+1365_-409+1369delinsGTGTT	XP_005273648.1:n.-409+1365_-409+1369delinsGTGTT
XM_011544596.3:c.254+1365_254+1369delinsGTGTT	XP_011542898.1:n.254+1365_254+1369delinsGTGTT
XM_011544597.3:c.254+1365_254+1369delinsGTGTT	XP_011542899.1:n.254+1365_254+1369delinsGTGTT
XM_011544598.2:c.-109+1365_-109+1369delinsGTGTT	XP_011542900.1:n.-109+1365_-109+1369delinsGTGTT
XM_011544601.3:c.-109+7757_-109+7761delinsGTGTT	XP_011542903.1:n.-109+7757_-109+7761delinsGTGTT
XM_017013706.2:c.-200+1019_-200+1023delinsGTGTT	XP_016869195.1:n.-200+1019_-200+1023delinsGTGTT
XM_017013710.1:c.-434+1365_-434+1369delinsGTGTT	XP_016869199.1:n.-434+1365_-434+1369delinsGTGTT
XM_017013714.2:c.-306+1365_-306+1369delinsGTGTT	XP_016869203.1:n.-306+1365_-306+1369delinsGTGTT
XM_024447214.1:c.-263+1365_-263+1369delinsGTGTT	XP_024302982.1:n.-263+1365_-263+1369delinsGTGTT
XM_024447215.1:c.-354+1365_-354+1369delinsGTGTT	XP_024302983.1:n.-354+1365_-354+1369delinsGTGTT
XM_024447216.1:c.-378+1365_-378+1369delinsGTGTT	XP_024302984.1:n.-378+1365_-378+1369delinsGTGTT
XM_024447219.1:c.-1098+1365_-1098+1369delinsGTGTT	XP_024302987.1:n.-1098+1365_-1098+1369delinsGTGTT
NM_020844.3:c.-200+7757_-200+7761delinsGTGTT MANE Select	NP_065895.2:n.-200+7757_-200+7761delinsGTGTT